510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K982639Substantially Equivalent

Spife Urine Ife

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

K982639 is the FDA 510(k) clearance record for SPIFE URINE IFE, a class II device, cleared for Helena Laboratories on under FDA product code DAO (Igm (Mu Chain Specific), Antigen, Antiserum, Control). FDA records list 282 510(k) clearances for Helena Laboratories, from to . As of , FDA records show no recalls naming K982639.

Clearance record

Decision date
Received
(98 days to decision)
Product code
DAO Igm (Mu Chain Specific), Antigen, Antiserum, Control
Regulation
21 CFR 866.5550
Device class
Class II
Review panel
Immunology
Applicant
Helena Laboratories 1530 Lindbergh Dr., Beaumont TX
510(k) summary
Statement
Third party review
No

Clearances, product code DAO

Trailing 12 months

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

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