# Klein-Baker Medical, Inc.

- Location (FDA's records): San Antonio, TX
- FDA decisions: 5 (1996–1997): 5 510(k) clearances
- Product codes: FOZ (1), MIA (1), LJS (1), KDJ (1), FOS (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Pneumrx, Inc.: 1 (https://510kreport.com/company/pneumrx)
- Kendall: 1 (https://510kreport.com/company/kendall)

## Its most-cited devices
- K970997: Neo-Care Lumber Puncture Kit (1997), cited by 1
- K970434: Neo-Picc (1997), cited by 1

## Recent decisions
- K972731: Neo-Care Peritoneal Dialysis Administration Set (Sep 29, 1997)
- K970997: Neo-Care Lumber Puncture Kit (May 22, 1997)
- K970434: Neo-Picc (Apr 1, 1997)
- K963972: Neo-Care Dual Lumen Umbilical Catheter (Dec 24, 1996)
- K963867: Neo-Care Catheterization Tray (Nov 6, 1996)

Source page: https://510kreport.com/company/klein-baker-medical