Single Use Hot Biopsy Forceps FD-231— 510(k) K171916
Substantially EquivalentOlympus Medical Systems Corp.
FDA 510(k) clearance K171916 for Single Use Hot Biopsy Forceps FD-231, Substantially Equivalent on 2017-10-13. Applicant: Olympus Medical Systems Corp.. Device class: 2.
Clearance details
- Applicant
- Olympus Medical Systems Corp.
- Product code
- Code KGE
- Device class
- Class 2
- Regulation
- 21 CFR 876.4300
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hachioji-Shi, JP
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Data sourced from openFDA. This site is unofficial and independent of the FDA.