# Bio Clinic Co.

- Location (FDA's records): St. Louis, MI
- FDA decisions: 14 (1988–1993): 14 510(k) clearances
- Product codes: IOQ (4), JHI (3), FNM (2), CEP (1), JLW (1), CGJ (1), CFT (1), FMF (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
- K930791: American Power Conversions, Back-Ups 600 (Aug 6, 1993)
- K932480: PRISM (Jul 21, 1993)
- K926189: Orthoderm Consummate Air Therapy Bed W/Scale (Jun 24, 1993)
- K921958: Elisa Tube TSH Test (Jul 2, 1992)
- K922140: Orthoderm Convertible II (May 27, 1992)
- K921212: Mirco Elisa HPL Test Kit (May 7, 1992)
- K921211: Now Pregnancy Test Kit (May 7, 1992)
- K920920: Elisa Tube LH Test Kit (Apr 8, 1992)

Source page: https://510kreport.com/company/bio-clinic