510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K812139Substantially Equivalent

Vacuum Suction Filter

K & G Healthcare Ind., Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K812139 is the FDA 510(k) clearance record for VACUUM SUCTION FILTER, a class II device, cleared for K & G Healthcare Ind., Inc. on under FDA product code KDQ (Bottle, Collection, Vacuum). FDA records list 3 510(k) clearances for K & G Healthcare Ind., Inc., from to . As of , FDA records show no recalls naming K812139.

Clearance record

Decision date
Received
(23 days to decision)
Product code
KDQ Bottle, Collection, Vacuum
Regulation
21 CFR 880.6740
Device class
Class II
Review panel
General Hospital
Applicant
K & G Healthcare Ind., Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KDQ

Trailing 12 months

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

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