GENERAL UTILITY SURG. SCISSORS #460180-— 510(k) K800721
Substantially EquivalentEdward Weck, Inc.
FDA 510(k) clearance K800721 for GENERAL UTILITY SURG. SCISSORS #460180-, Substantially Equivalent on 1980-05-08. Applicant: Edward Weck, Inc.. Device class: 1.
Clearance details
- Applicant
- Edward Weck, Inc.
- Product code
- Code HRR
- Device class
- Class 1
- Regulation
- 21 CFR 888.4540
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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