SUTURE REMOVAL KIT— 510(k) K855131
Substantially EquivalentDynarex Corp.
FDA 510(k) clearance K855131 for SUTURE REMOVAL KIT, Substantially Equivalent on 1986-01-13. Applicant: Dynarex Corp.. Device class: 1.
Clearance details
- Applicant
- Dynarex Corp.
- Product code
- Code JOK
- Device class
- Class 1
- Regulation
- 21 CFR 880.6820
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Brewster, NY, US
Recent devices under product code JOK
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Data sourced from openFDA. This site is unofficial and independent of the FDA.