KAPPLER PRO/VENT PROCEDURE GOWN— 510(k) K932694
Substantially EquivalentKappler, Inc.
FDA 510(k) clearance K932694 for KAPPLER PRO/VENT PROCEDURE GOWN, Substantially Equivalent on 1994-03-29. Applicant: Kappler, Inc.. Device class: 2.
Clearance details
- Applicant
- Kappler, Inc.
- Product code
- Code FYA
- Device class
- Class 2
- Regulation
- 21 CFR 878.4040
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Guntersville, AL, US
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More clearances from Kappler, Inc.
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