510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K883306Substantially Equivalent

Binas Luteinizing Hormone Irma Test Kit

Binax, Inc., S. Portland ME / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K883306 is the FDA 510(k) clearance record for BINAS LUTEINIZING HORMONE IRMA TEST KIT, a class II device, cleared for Binax, Inc. on under FDA product code JIT (Calibrator, Secondary). FDA records list 10 510(k) clearances for Binax, Inc., from to . As of , FDA records show no recalls naming K883306.

Clearance record

Decision date
Received
(63 days to decision)
Product code
JIT Calibrator, Secondary
Regulation
21 CFR 862.1150
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Binax, Inc. 95 Darling Ave., S. Portland ME
Third party review
No

Clearances, product code JIT

Trailing 12 months

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

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