510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K952667Substantially Equivalent

Chrom Z-Heparin, Cat. No 5242

Helena Laboratories, Corp., Beaumont TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K952667 is the FDA 510(k) clearance record for CHROM Z-HEPARIN, CAT. NO 5242, a class II device, cleared for Helena Laboratories on under FDA product code KFF (Assay, Heparin). FDA records list 282 510(k) clearances for Helena Laboratories, from to . As of , FDA records show no recalls naming K952667.

Clearance record

Decision date
Received
(247 days to decision)
Product code
KFF Assay, Heparin
Regulation
21 CFR 864.7525
Device class
Class II
Review panel
Hematology
Applicant
Helena Laboratories 1530 Lindbergh Dr., Beaumont TX
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