HD Camera Head OLYMPUS CH-S200-08-LB
Olympus Medical Systems Corporation · K261260
FDA-authorized Predetermined Change Control Plan
- Company
- Olympus Medical Systems Corporation
- 510(k)/De Novo #
- K261260
- Decision date
- 2026-06-24
- Panel
- Gastroenterology, Urology
- Pathway
- 510(k)
- Category
- Non-AI
- PCCP type
- Compatibility expansion
- Monitoring commitment
- Not stated
What this PCCP covers. Permits compatibility expansion to additional hardware
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We read the PCCP for HD Camera Head OLYMPUS CH-S200-08-LB, then map the post-market monitoring that its modification protocol requires, including the deployment-period evidence most teams can't reconstruct at modification time. Sentir is the independent system of record that produces it.
Book a callSource: U.S. FDA public records (openFDA 510(k)/De Novo databases and accessdata.fda.gov). PCCP type and category are editorial classifications based on public documents, not official FDA designations.
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