GREER DERMAPIK SYSTEM— 510(k) K890360
Substantially EquivalentGreer Laboratories, Inc.
FDA 510(k) clearance K890360 for GREER DERMAPIK SYSTEM, Substantially Equivalent on 1989-06-23. Applicant: Greer Laboratories, Inc.. Device class: 2.
Clearance details
- Applicant
- Greer Laboratories, Inc.
- Product code
- Code SCL
- Device class
- Class 2
- Regulation
- 21 CFR 880.5570
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Lenoir, NC, US
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