DEXIDE LAPAROSCOPIC KITS— 510(k) K924117
UnknownDexide, Inc.
FDA 510(k) clearance K924117 for DEXIDE LAPAROSCOPIC KITS, Unknown on 1993-03-23. Applicant: Dexide, Inc.. Device class: 1.
Clearance details
- Applicant
- Dexide, Inc.
- Product code
- Code KDD
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Fort Worth, TX, US
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