510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K953247Substantially Equivalent

Gibson Id A.e. Test

Microbiologics, Inc., Lexington KY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K953247 is the FDA 510(k) clearance record for GIBSON ID A.E. TEST, a class I device, cleared for Gibson Laboratories, Inc. on under FDA product code JTO (Discs, Strips And Reagents, Microorganism Differentiation). FDA records list 22 510(k) clearances for MICROBIOLOGICS, INC., from to . As of , FDA records show no recalls naming K953247.

Clearance record

Decision date
Received
(132 days to decision)
Product code
JTO Discs, Strips And Reagents, Microorganism Differentiation
Regulation
21 CFR 866.2660
Device class
Class I
Review panel
Microbiology
Applicant
Gibson Laboratories, Inc. 1040 Manchester St., Lexington KY
510(k) summary
Statement
Third party review
No

Clearances, product code JTO

Trailing 12 months

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

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