# Medi-Spec

- Location (FDA's records): Mchenry, IL
- FDA decisions: 8 (1978–1984): 8 510(k) clearances
- Product codes: KKX (2), GEE (1), GAD (1), HHK (1), HMP (1), HDY (1), HIX (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
- K833068: Laminaria Japonica Cervical Dilator (Feb 4, 1984)
- K812694: Whisk-R (Oct 26, 1981)
- K812426: Uterine Aspiration Curettes (Rigid&Flex) (Oct 8, 1981)
- K801554: Sterile Cast Padding (Aug 4, 1980)
- K800404: Medspec Operative Opthalmic Kit (Apr 24, 1980)
- K800490: Sterile Dressing Pack (Mar 12, 1980)
- K790952: Clamp Covers (Jun 5, 1979)
- K780548: Disposa-Loops (Aug 21, 1978)

Source page: https://510kreport.com/company/medi-spec