510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K812274Substantially Equivalent

Auramine O Mycrobacterial Stain Set

Carr-Scarborough Microbiologicals, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K812274 is the FDA 510(k) clearance record for AURAMINE O MYCROBACTERIAL STAIN SET, a class I device, cleared for Carr-Scarborough Microbiologicals, Inc. on under FDA product code KJK (Auramine O). FDA records list 24 510(k) clearances for Carr-Scarborough Microbiologicals, Inc., from to . As of , FDA records show no recalls naming K812274.

Clearance record

Decision date
Received
(19 days to decision)
Product code
KJK Auramine O
Regulation
21 CFR 864.1850
Device class
Class I
Review panel
Hematology
Applicant
Carr-Scarborough Microbiologicals, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KJK

Trailing 12 months

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

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