EPISIOTOMY SCISSORS
FDA 510(k) clearance K854900 · decided 1985-12-24
Clearance details
- K-number
- K854900
- Device name
- EPISIOTOMY SCISSORS
- Applicant
- Euro-Med Intl.
- Decision
- Substantially Equivalent
- Date received
- 1985-12-06
- Decision date
- 1985-12-24
- Days to decision
- 18 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Danville, CA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.