510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K885131Substantially Equivalent

Kit Pak Suction Catheter Kit

Kit Pak, Inc., Elk Grove Village IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K885131 is the FDA 510(k) clearance record for KIT PAK SUCTION CATHETER KIT, a class I device, cleared for Kit Pak, Inc. on under FDA product code BSY (Catheters, Suction, Tracheobronchial). FDA records list 13 510(k) clearances for Kit Pak, Inc., from to . As of , FDA records show no recalls naming K885131.

Clearance record

Decision date
Received
(28 days to decision)
Product code
BSY Catheters, Suction, Tracheobronchial
Regulation
21 CFR 868.6810
Device class
Class I
Review panel
Anesthesiology
Applicant
Kit Pak, Inc. 825 Chase Ave., Elk Grove Village IL
Third party review
No

Clearances, product code BSY

Trailing 12 months

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

FDA records show no clearances under product code BSY in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code BSY, 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