510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K872698Substantially Equivalent

Adenovirus Cf Antigen and Control Antigen

Sita, Inc., Allentown NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K872698 is the FDA 510(k) clearance record for ADENOVIRUS CF ANTIGEN AND CONTROL ANTIGEN, a class I device, cleared for Sita, Inc. on under FDA product code GOA (Antisera, Cf, Adenovirus 1-33). FDA records list 9 510(k) clearances for Sita, Inc., from to . As of , FDA records show no recalls naming K872698.

Clearance record

Decision date
Received
(73 days to decision)
Product code
GOA Antisera, Cf, Adenovirus 1-33
Regulation
21 CFR 866.3020
Device class
Class I
Review panel
Microbiology
Applicant
Sita, Inc. Regulatory Affairs Dept., Allentown NJ
Third party review
No

Clearances, product code GOA

Trailing 12 months

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

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