510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K050367Substantially Equivalent

Biophen Heparin 3, Biophen Heparin 6

Hyphen Biomed Sasu, Mason OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K050367 is the FDA 510(k) clearance record for BIOPHEN HEPARIN 3, BIOPHEN HEPARIN 6, a class II device, cleared for Hyphen Biomed on under FDA product code KFF (Assay, Heparin). FDA records list 6 510(k) clearances for HYPHEN BIOMED SASU, from to . As of , FDA records show no recalls naming K050367.

Clearance record

Decision date
Received
(464 days to decision)
Product code
KFF Assay, Heparin
Regulation
21 CFR 864.7525
Device class
Class II
Review panel
Hematology
Applicant
Hyphen Biomed 6560 Gove Ct., Mason OH
510(k) summary
Statement
Third party review
No

Clearances, product code KFF

Trailing 12 months
1 clearance under product code KFF in the twelve months to October 2026, September 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code KFF, 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 20261
October 20260