510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K872699Substantially Equivalent

Mumps Cf Antigen and Control Antigen

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

K872699 is the FDA 510(k) clearance record for MUMPS CF ANTIGEN AND CONTROL ANTIGEN, a class I device, cleared for Sita, Inc. on under FDA product code GRB (Antiserum, Cf, Mumps Virus). FDA records list 9 510(k) clearances for Sita, Inc., from to . As of , FDA records show no recalls naming K872699.

Clearance record

Decision date
Received
(73 days to decision)
Product code
GRB Antiserum, Cf, Mumps Virus
Regulation
21 CFR 866.3380
Device class
Class I
Review panel
Microbiology
Applicant
Sita, Inc. Regulatory Affairs Dept., Allentown NJ
Third party review
No

Clearances, product code GRB

Trailing 12 months

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

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