STERILE SUTURE REMOVAL KIT— 510(k) K821502
Substantially EquivalentPro-Pak
FDA 510(k) clearance K821502 for STERILE SUTURE REMOVAL KIT, Substantially Equivalent on 1982-07-09. Applicant: Pro-Pak. Device class: 1.
Clearance details
- Applicant
- Pro-Pak
- 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 Pro-Pak
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