# J.J. Skinner, Inc.

- Location (FDA's records): Great Neck, NY
- FDA decisions: 7 (1990–1996): 7 510(k) clearances
- Product codes: LRO (2), LRP (1), FKG (1), FRG (1), GJE (1), FOZ (1)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Its most-cited devices
- K903545: Carekits (TM), IV/Cath/Cent Line Dress/TPN/CVP Kits (1990), cited by 1

## Recent decisions
- K961227: JJ Skinner Carekits Wound Care Management/Dressing Change Tray (Jun 10, 1996)
- K961683: JJ Skinner Carekits  Minor Surgical Procedure Tray (May 10, 1996)
- K925469: JJ Skinner Carekits (TM) Dialysis on/Off Kit (May 3, 1995)
- K925467: JJ Skinner Carekits (TM) Dry/Wet/Gel Skin Scrub Kit (May 11, 1994)
- K925468: JJ Skinner Carekits (TM) Blood Collection Kit (Apr 11, 1994)
- K903545: Carekits (TM), IV/Cath/Cent Line Dress/TPN/CVP Kits (Nov 13, 1990)
- K903544: Carekits (TM) Incision/Drainage/Suture Removal Kits (Aug 31, 1990)

Source page: https://510kreport.com/company/jj-skinner