# E.M. Adams

- Location (FDA's records): Mchenry, IL
- FDA decisions: 23 (1978–1997): 23 510(k) clearances
- Names in FDA's records: E.M. Adams (21); E.M. Adams Co., Inc. (2)
- Product codes: FSM (3), EFQ (2), EAJ (2), FMQ (2), KDD (2), FZZ (1), FZI (1), KYZ (1), GEN (1), FPP (1), MCZ (1), FZT (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
- K971948: Patient Restraint (Aug 6, 1997)
- K971536: Restraints (Vests and Jackets) (Jul 1, 1997)
- K905173: Splash Guard (Apr 25, 1991)
- K910468: Sterile Disposable Drape (S) (Mar 21, 1991)
- K873978: Disposable Bipolar Forceps (Nov 23, 1987)
- K850063: Instrument Pocket (Feb 21, 1985)
- K843724: I.V. Start Kit & Obstetrical Kit (Jan 10, 1985)
- K843783: Wet Pack (Dec 19, 1984)

Source page: https://510kreport.com/company/em-adams