FORCEPS— 510(k) K904723
Substantially EquivalentMinto Research & Development, Inc.
FDA 510(k) clearance K904723 for FORCEPS, Substantially Equivalent on 1991-07-26. Applicant: Minto Research & Development, Inc.. Device class: 1.
Clearance details
- Applicant
- Minto Research & Development, Inc.
- Product code
- Code GEN
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Redding, CA, US
Recent devices under product code GEN
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