510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K821011Substantially Equivalent

Ace Activity Microvial Test Set

Ventrex Laboratories, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K821011 is the FDA 510(k) clearance record for ACE ACTIVITY MICROVIAL TEST SET, a class II device, cleared for Ventrex Laboratories, Inc. on under FDA product code KQN (Radioassay, Angiotensin Converting Enzyme). FDA records list 82 510(k) clearances for Ventrex Laboratories, Inc., from to . As of , FDA records show no recalls naming K821011.

Clearance record

Decision date
Received
(21 days to decision)
Product code
KQN Radioassay, Angiotensin Converting Enzyme
Regulation
21 CFR 862.1090
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Ventrex Laboratories, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KQN

Trailing 12 months

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

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