510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K820177Substantially Equivalent

Coagulase Plasma

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

K820177 is the FDA 510(k) clearance record for COAGULASE PLASMA, a class I device, cleared for Quadroma, Inc. on under FDA product code JTL (Plasma, Coagulase, Human, Horse And Rabbit). FDA records list one 510(k) clearance for Quadroma, Inc. As of , FDA records show no recalls naming K820177.

Clearance record

Decision date
Received
(14 days to decision)
Product code
JTL Plasma, Coagulase, Human, Horse And Rabbit
Regulation
21 CFR 866.2160
Device class
Class I
Review panel
Microbiology
Applicant
Quadroma, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code JTL

Trailing 12 months

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

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