510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K843654Substantially Equivalent

Chlamydia

Institute Virion, Ltd., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K843654 is the FDA 510(k) clearance record for CHLAMYDIA, a class I device, cleared for Institute Virion , Ltd. on under FDA product code GPW (Antigen, Cf, Psittacosis (Chlamydia Group)). FDA records list 16 510(k) clearances for Institute Virion , Ltd., from to . As of , FDA records show no recalls naming K843654.

Clearance record

Decision date
Received
(325 days to decision)
Product code
GPW Antigen, Cf, Psittacosis (Chlamydia Group)
Regulation
21 CFR 866.3120
Device class
Class I
Review panel
Microbiology
Applicant
Institute Virion , Ltd. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code GPW

Trailing 12 months

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

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