510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K760835Substantially Equivalent

Anti-Aspergillus Cont. Ser. (Mycelial)

I M, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K760835 is the FDA 510(k) clearance record for ANTI-ASPERGILLUS CONT. SER. (MYCELIAL), a class I device, cleared for I M, Inc. on under FDA product code KFG (Antiserum, Positive Control, Aspergillus Spp.). FDA records list 26 510(k) clearances for I M, Inc., from to . As of , FDA records show no recalls naming K760835.

Clearance record

Decision date
Received
(19 days to decision)
Product code
KFG Antiserum, Positive Control, Aspergillus Spp.
Regulation
21 CFR 866.3040
Device class
Class I
Review panel
Microbiology
Applicant
I M, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KFG

Trailing 12 months

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

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