PARALLEL ACTION PLIERS— 510(k) K861953
Substantially EquivalentMed-Tool, Inc.
FDA 510(k) clearance K861953 for PARALLEL ACTION PLIERS, Substantially Equivalent on 1986-06-06. Applicant: Med-Tool, Inc.. Device class: 1.
Clearance details
- Applicant
- Med-Tool, Inc.
- Product code
- Code HTC
- 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
- St. Louis, MO, US
Recent devices under product code HTC
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