510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K872677Substantially Equivalent

Iafp B.h.i. Agar

I.A.F. Production, Inc., Laval, Que. H7n-423, CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K872677 is the FDA 510(k) clearance record for IAFP B.H.I. AGAR, a class I device, cleared for I.A.F. Production, Inc. on under FDA product code JSG (Culture Media, Non-Selective And Non-Differential). FDA records list 29 510(k) clearances for I.A.F. Production, Inc., from to . As of , FDA records show no recalls naming K872677.

Clearance record

Decision date
Received
(31 days to decision)
Product code
JSG Culture Media, Non-Selective And Non-Differential
Regulation
21 CFR 866.2300
Device class
Class I
Review panel
Microbiology
Applicant
I.A.F. Production, Inc. 527, Boul. Des Prairies, Laval, Que. H7n-423, CA
Third party review
No

Clearances, product code JSG

Trailing 12 months

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

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