THE S.A.F.E. SYSTEM— 510(k) K880890
Substantially EquivalentPfizer Laser Systems
FDA 510(k) clearance K880890 for THE S.A.F.E. SYSTEM, Substantially Equivalent on 1988-05-11. Applicant: Pfizer Laser Systems. Device class: 2.
Clearance details
- Applicant
- Pfizer Laser Systems
- 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
- Irvine, CA, US
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