# U.S. Mfg. & Management, Inc.

- Location (FDA's records): San Bernardino, CA
- FDA decisions: 5 (1984–1992): 5 510(k) clearances
- Product codes: KMK (1), BXB (1), KSS (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K920860: Controlled Passive Motion Machine (Apr 2, 1992)
- K874436: Fluid Sampling Pack (Jan 5, 1988)
- K862335: Modified I.V. Start, RE-Start, Pedi and Geri-Kit (Jul 24, 1986)
- K853242: I.V. Start Kit, I.V. Restart Kit, Pedi-Kit,Geri-KI (Aug 30, 1985)
- K842999: Veni-Shield (Sep 24, 1984)

Source page: https://510kreport.com/company/us-mfg-management