# Johnson & Johnson Patient Care, Inc.

- Location (FDA's records): New Brunswick, NJ
- FDA decisions: 4 (1988–1989): 4 510(k) clearances
- Product codes: FRO (2), KYZ (1), KMK (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Shippert Medical Technologies Corp.: 1 (https://510kreport.com/company/shippert-medical-technologies)

## Its most-cited devices
- K884749: Johnson & Johnson Sterile Spray Tip Syringe (1988), cited by 1

## Recent decisions
- K895431: Johnson & Johnson Tube Securement Device (Oct 13, 1989)
- K892851: Actisorb* Plus Activated Charcoal Dress W/Silver (Sep 26, 1989)
- K890545: NU-Derm Hydrocolloid Dressing (Mar 23, 1989)
- K884749: Johnson & Johnson Sterile Spray Tip Syringe (Dec 15, 1988)

Source page: https://510kreport.com/company/johnson-johnson-patient-care