510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K970120Substantially Equivalent

Bile Acids Reagent Set

Teco Diagnostics, Anaheim CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K970120 is the FDA 510(k) clearance record for BILE ACIDS REAGENT SET, a class II device, cleared for Teco Diagnostics on under FDA product code KWW (Radioimmunoassay, Cholyglycine, Bile Acids). FDA records list 55 510(k) clearances for Teco Diagnostics, from to . As of , FDA records show no recalls naming K970120.

Clearance record

Decision date
Received
(69 days to decision)
Product code
KWW Radioimmunoassay, Cholyglycine, Bile Acids
Regulation
21 CFR 862.1177
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Teco Diagnostics 4925 E. Hunter Ave., Anaheim CA
510(k) summary
Statement
Third party review
No

Clearances, product code KWW

Trailing 12 months

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

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