510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K913906Substantially Equivalent

Q Fever Igg Ifa Test

Hillcrest Biologicals, Cypress CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K913906 is the FDA 510(k) clearance record for Q FEVER IGG IFA TEST, a class I device, cleared for Hillcrest Biologicals on under FDA product code GPJ (Antiserum, Fluorescent, Q Fever). FDA records list 33 510(k) clearances for Hillcrest Biologicals, from to . As of , FDA records show no recalls naming K913906.

Clearance record

Decision date
Received
(418 days to decision)
Product code
GPJ Antiserum, Fluorescent, Q Fever
Regulation
21 CFR 866.3500
Device class
Class I
Review panel
Microbiology
Applicant
Hillcrest Biologicals 10703 Progress Way, Cypress CA
510(k) summary
Statement
Third party review
No

Clearances, product code GPJ

Trailing 12 months

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

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