510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K972706Substantially Equivalent

Clinitek Microalbumin Reagent Strips

Bayer Corp., Elkhart IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K972706 is the FDA 510(k) clearance record for CLINITEK MICROALBUMIN REAGENT STRIPS, a class II device, cleared for Bayer Corp. on under FDA product code CJG (Tetrabromo-M-Cresolsulfonphthalein, Albumin). FDA records list 20 510(k) clearances for Bayer Corp., from to . As of , FDA records show no recalls naming K972706.

Clearance record

Decision date
Received
(50 days to decision)
Product code
CJG Tetrabromo-M-Cresolsulfonphthalein, Albumin
Regulation
21 CFR 862.1035
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Bayer Corp. 1884 Miles Ave., Elkhart IN
510(k) summary
Summary
Third party review
No

Clearances, product code CJG

Trailing 12 months

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

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