510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K870945Substantially Equivalent

Rabbit Plasma Fibrinogen Supplement Sr 122

Oxoid U.S.A., Inc., Columbia MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K870945 is the FDA 510(k) clearance record for RABBIT PLASMA FIBRINOGEN SUPPLEMENT SR 122, a class I device, cleared for Oxoid U.S.A., Inc. on under FDA product code JTL (Plasma, Coagulase, Human, Horse And Rabbit). FDA records list 93 510(k) clearances for Oxoid U.S.A., Inc., from to . As of , FDA records show no recalls naming K870945.

Clearance record

Decision date
Received
(93 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
Oxoid U.S.A., Inc. 9017 Red Branch Rd., Columbia MD
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