SUTURE REMOVAL TRAY— 510(k) K820423
Substantially EquivalentMegaplast, Inc.
FDA 510(k) clearance K820423 for SUTURE REMOVAL TRAY, Substantially Equivalent on 1982-03-10. Applicant: Megaplast, Inc.. Device class: 1.
Clearance details
- Applicant
- Megaplast, Inc.
- Product code
- Code KDD
- 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
- Mchenry, IL, US
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More clearances from Megaplast, Inc.
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