510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K830127Substantially Equivalent

Quik-Dip Blood Stain

Mercedes Scientific Co., Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K830127 is the FDA 510(k) clearance record for QUIK-DIP BLOOD STAIN, a class I device, cleared for Mercedes Scientific Co., Inc. on under FDA product code IAF (Wright'S Stain). FDA records list 2 510(k) clearances for Mercedes Scientific Co., Inc., from to . As of , FDA records show no recalls naming K830127.

Clearance record

Decision date
Received
(34 days to decision)
Product code
IAF Wright'S Stain
Regulation
21 CFR 864.1850
Device class
Class I
Review panel
Hematology
Applicant
Mercedes Scientific Co., Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code IAF

Trailing 12 months

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

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