# Fisher Scientific Co., LLC

- Location (FDA's records): Mchenry, IL
- FDA decisions: 90 (1976–1993): 89 510(k) clearances and 1 original PMA approval
- Product codes: CHL (15), JPK (5), JJY (5), DIF (4), JGS (3), CEK (2), JPI (2), JIT (2), GKF (2), JJS (2), JHS (2), CIX (2)
- 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
- K930415: Microhematocrit Rotor (Mar 23, 1993)
- K915825: Marathon 6K General-Purpose Centrifuge (Mar 11, 1992)
- K915441: Marathon 13K/H Microhematocrit Centrifuge (Jan 8, 1992)
- K890534: Modified Uriqual (TM) Urinalysis Control Level 1 (Mar 8, 1989)
- K881275: Uriqual (TM) Urinalysis Controls (Human) I & II (May 16, 1988)
- K874054: Fisher Diagnostics Hematall Iii Las Reagent (Oct 20, 1987)
- K872916: Histomatic Slide Stainer, Code-on Version (Sep 14, 1987)
- K871058: Serachem Liquid Spinal Fluid Control (Human) (Apr 6, 1987)

Source page: https://510kreport.com/company/fisher-scientific