# I M, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 41 (1976–1992): 41 510(k) clearances
- Product codes: GMJ (2), FMF (2), GMG (2), GMK (2), HRQ (2), LDQ (1), GMH (1), KFH (1), JWT (1), HBA (1), KOD (1), FRN (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
- Precision Dynamics Corp.: 1 (https://510kreport.com/company/precision-dynamics)

## Its most-cited devices
- K880753: Umbilical Cord Clamp (1988), cited by 1

## Recent decisions
- K914600: Neurological Sponge (Dec 30, 1992)
- K892389: Biopsy Kit (Jul 17, 1989)
- K881363: Syringe Prefilled with Water (Jun 23, 1988)
- K880753: Umbilical Cord Clamp (Apr 27, 1988)
- K872741: Nutripump (Oct 20, 1987)
- K871495: Bandages Catalog Number: 101 to 220 (May 8, 1987)
- K863785: Makler Catheter (Dec 11, 1986)
- K854155: Sterile Saline Solution (Dec 10, 1985)

Source page: https://510kreport.com/company/i-m
