# Pollak (Intl.), Ltd.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 31 (1980–2000): 31 510(k) clearances
- Product codes: EFQ (4), FMC (2), KGX (2), FQM (2), KXF (2), KDD (2), HMP (1), FRQ (1), KNX (1), FLN (1), NAB (1), NAD (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
- K000227: Umbicut (Apr 27, 2000)
- K810049: Pedicat* (Apr 21, 1981)
- K810050: Vecafix* (Mar 26, 1981)
- K802011: Infussion Alarm System I.a.S. Cat.#1118 (Oct 31, 1980)
- K802009: Flowclamp Cat.#1011 & 1012 (Oct 31, 1980)
- K802017: Dressing Change Set Cat.#910-930 (Oct 10, 1980)
- K802007: Pediwet=Guaze Impregnated with Petrol (Sep 26, 1980)
- K802022: Sterile Guaze Swabs Cat.#301-420 (Sep 16, 1980)

Source page: https://510kreport.com/company/pollak-intl