BEIJING GOLDENLASER DEVELOPMENT CO., LTD. · 89-08 · CHINA
For BEIJING GOLDENLASER DEVELOPMENT CO., LTD., import alert is 89-08; country is CHINA; import alert name is "Detention Without Physical Examination of Devices without Approved PMA's or IDE's and Other Devices Not Substantially Equivalent or Without a 510(k)"; product is GL029 RF Cavitation Equipment | GL029 RF Cavitation Equipment; product code is 89 I - - LX Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat | 89 I - - SA Massager, Therapeutic, Electric; date published is 05/29/2012; address is 1st Floor # 339 , Shenwei North Rd; Yanjiaozhen Sanhe , Langfang, Hebei CHINA, verified against its source on 2026-09-30.
- Firm
- BEIJING GOLDENLASER DEVELOPMENT CO., LTD. verified
- Import alert
- 89-08
- Import alert name
- "Detention Without Physical Examination of Devices without Approved PMA's or IDE's and Other Devices Not Substantially Equivalent or Without a 510(k)"
- Country
- CHINA verified
- Address
- 1st Floor # 339 , Shenwei North Rd; Yanjiaozhen Sanhe , Langfang, Hebei CHINA verified
- Date published
- 05/29/2012 verified
- Product code
- 89 I - - LX Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat | 89 I - - SA Massager, Therapeutic, Electric each item verified
- Product
- GL029 RF Cavitation Equipment | GL029 RF Cavitation Equipment each item verified
- FDA notes
- Class; Unknown | Class; Unknown each item verified
What the source says
BEIJING GOLDENLASER DEVELOPMENT CO., LTD. Date Published : 05/29/2012 1st Floor # 339 , Shenwei North Rd; Yanjiaozhen Sanhe , Langfang, Hebei CHINA
— accessdata.fda.gov, retrieved 2026-09-15
Where each value comes from
The values above are stated away from the sentence quoted with the answer, so the passage that states them is shown here too.
Product code, Product and FDA notes
89 I - - LX Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat Date Published: 05/29/2012 Desc: GL029 RF Cavitation Equipment Notes: Class; Unknown 89 I - - SA Massager, Therapeutic, Electric Date Published: 05/29/2012 Desc: GL029 RF Cavitation Equipment Notes: Class; Unknown
— all from accessdata.fda.gov, retrieved 2026-09-15
Source
- accessdata.fda.govhttps://www.accessdata.fda.gov/cms_ia/importalert_244.html