510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K854245Substantially Equivalent

Sigma Angiotensin Converting Enzyme 305-UV

Sigma Diagnostics, Inc., St. Louis MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K854245 is the FDA 510(k) clearance record for SIGMA ANGIOTENSIN CONVERTING ENZYME 305-UV, a class II device, cleared for Sigma Diagnostics, Inc. on under FDA product code KQN (Radioassay, Angiotensin Converting Enzyme). FDA records list 164 510(k) clearances for Sigma Diagnostics, Inc., from to . As of , FDA records show no recalls naming K854245.

Clearance record

Decision date
Received
(93 days to decision)
Product code
KQN Radioassay, Angiotensin Converting Enzyme
Regulation
21 CFR 862.1090
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Sigma Diagnostics, Inc. P.O. Box 14508, St. Louis MO
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