NINJA SCALPEL— 510(k) K873493
Substantially EquivalentPrimrose Medical, Inc.
FDA 510(k) clearance K873493 for NINJA SCALPEL, Substantially Equivalent on 1987-09-24. Applicant: Primrose Medical, Inc.. Device class: 1.
Clearance details
- Applicant
- Primrose Medical, Inc.
- Product code
- Code GES
- 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
- Woburn, MA, US
Recent devices under product code GES
view allMore clearances from Primrose Medical, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.