510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K871545Substantially Equivalent

New Fuchsin Solution

Sigma Diagnostics, Inc., St. Louis MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K871545 is the FDA 510(k) clearance record for NEW FUCHSIN SOLUTION, a class I device, cleared for Sigma Diagnostics, Inc. on under FDA product code IDF (Acid, Fuchsin). FDA records list 164 510(k) clearances for Sigma Diagnostics, Inc., from to . As of , FDA records show no recalls naming K871545.

Clearance record

Decision date
Received
(15 days to decision)
Product code
IDF Acid, Fuchsin
Regulation
21 CFR 864.1850
Device class
Class I
Review panel
Hematology
Applicant
Sigma Diagnostics, Inc. P.O. Box 14508, St. Louis MO
Third party review
No

Clearances, product code IDF

Trailing 12 months

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

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