CAREKITS(TM) INCISION/DRAINAGE/SUTURE REMOVAL KITS— 510(k) K903544
UnknownJ.J. Skinner, Inc.
FDA 510(k) clearance K903544 for CAREKITS(TM) INCISION/DRAINAGE/SUTURE REMOVAL KITS, Unknown on 1990-08-31. Applicant: J.J. Skinner, Inc.. Device class: 1.
Clearance details
- Applicant
- J.J. Skinner, Inc.
- Product code
- Code LRP
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Great Neck, NY, US
Recent devices under product code LRP
view allMore clearances from J.J. Skinner, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.