QUINEVAC II— 510(k) K920629
Substantially EquivalentRecto Molded Products, Inc.
FDA 510(k) clearance K920629 for QUINEVAC II, Substantially Equivalent on 1993-03-24. Applicant: Recto Molded Products, Inc.. Device class: 2.
Clearance details
- Applicant
- Recto Molded Products, Inc.
- Product code
- Code FYD
- Device class
- Class 2
- Regulation
- 21 CFR 878.5070
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
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