Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K801999Substantially Equivalent

Guaze Balls Cat.#601-720

Pollak (Intl.).ltd, Mchenry IL / Traditional, Substantially Equivalent

K801999 is the FDA 510(k) clearance record for GUAZE BALLS CAT.#601-720, cleared for Pollak (Intl.), Ltd. on under FDA product code EFQ (Gauze/Sponge, Internal). FDA records list 31 510(k) clearances for Pollak (Intl.), Ltd., from to . As of , FDA records show no recalls naming K801999.

Clearance record

Decision date
Received
(27 days to decision)
Product code
EFQ Gauze/Sponge, Internal
Device class
Unclassified
Review panel
Unknown
Applicant
Pollak (Intl.), Ltd. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code EFQ

Trailing 12 months

FDA records hold no clearances under product code EFQ in the trailing twelve months.

FDA records show no clearances under product code EFQ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EFQ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260