NEEDLE-GRABBER— 510(k) K923840
Substantially EquivalentGuardian Angel Products, Inc.
FDA 510(k) clearance K923840 for NEEDLE-GRABBER, Substantially Equivalent on 1993-07-13. Applicant: Guardian Angel Products, Inc.. Device class: 1.
Clearance details
- Applicant
- Guardian Angel Products, Inc.
- Product code
- Code GDF
- 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
- Washington, DC, US
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