510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K023091Substantially Equivalent

St Aia-Pack Testosterone Assay

Tosoh Medics, Inc., South San Francisco CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K023091 is the FDA 510(k) clearance record for ST AIA-PACK TESTOSTERONE ASSAY, a class I device, cleared for Tosoh Medics, Inc. on under FDA product code CDZ (Radioimmunoassay, Testosterones And Dihydrotestosterone). FDA records list 41 510(k) clearances for Tosoh Medics, Inc., from to . As of , FDA records show 3 recalls naming K023091.

Clearance record

Decision date
Received
(91 days to decision)
Product code
CDZ Radioimmunoassay, Testosterones And Dihydrotestosterone
Regulation
21 CFR 862.1680
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Tosoh Medics, Inc. 347 Oyster Pt. Blvd.,, South San Francisco CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code CDZ

Trailing 12 months
1 clearance under product code CDZ in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code CDZ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260