Federal Register 2026-16727 — effective 2026-09-16 — Hematology and Pathology Devices; Reclassification of In Situ Hybridization Test Systems for Use With a Corresponding Approved Oncology Therapeutic Product — Food and Drug Administration
What is the effective date for Federal Register 2026-16727 — effective 2026-09-16 — Hematology and Pathology Devices; Reclassification of In Situ Hybridization Test Systems for Use With a Corresponding Approved Oncology Therapeutic Product — Food and Drug Administration?
For Federal Register 2026-16727, effective date is 2026-09-16; agency is Food and Drug Administration; published is 2026-08-17; cfr parts amended is 21 CFR 864, recorded from its source on 2026-08-31; source re-checked 2026-09-16.
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— federalregister.gov, retrieved 2026-08-31
- FR document number
- 2026-16727 verified
- Rule
- Hematology and Pathology Devices; Reclassification of In Situ Hybridization Test Systems for Use With a Corresponding Approved Oncology Therapeutic Product verified
- Agency
- Food and Drug Administration verified
- Effective date
- 2026-09-16 verified
- DATES, as printed
- This order is effective September 16, 2026. See further discussion in section IV, "Implementation Strategy."
- CFR parts amended
- 21 CFR 864 our reading
- Published
- 2026-08-17 verified
Values marked our reading are our classification of what the source says — the source does not print them in those words. The quote below is the evidence for each one; judge it yourself.
Source
- federalregister.govhttps://www.federalregister.gov/api/v1/documents.json?per_page=1000&order=oldest&conditions%5Btype%5D%5B%5D=RULE&conditions%5Beffective_date%5D%5Bgte%5D=2026-08-31&conditions%5Beffective_date%5D%5Blte%5D=2026-12-31&fields%5B%5D=document_number&fields%5B%5D=title&fields%5B%5D=agency_names&fields%5B%5D=effective_on&fields%5B%5D=dates&fields%5B%5D=cfr_references&fields%5B%5D=publication_date&fields%5B%5D=html_url
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