510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
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K072141Substantially Equivalent

S40 Clinical Analyzer, S Test Ip, S Test Ua

Alfa Wassermann Diagnostic Technologies, Inc., West Caldwell NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K072141 is the FDA 510(k) clearance record for S40 CLINICAL ANALYZER, S TEST IP, S TEST UA, a class I device, cleared for Alfa Wassermann Diagnostic Technologies, Inc. on under FDA product code CEO (Phosphomolybdate (Colorimetric), Inorganic Phosphorus). FDA records list 23 510(k) clearances for Alfa Wassermann Diagnostic Technologies, Inc., from to . As of , FDA records show no recalls naming K072141.

Clearance record

Decision date
Received
(327 days to decision)
Product code
CEO Phosphomolybdate (Colorimetric), Inorganic Phosphorus
Regulation
21 CFR 862.1580
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Alfa Wassermann Diagnostic Technologies, Inc. 4 Henderson Dr., West Caldwell NJ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code CEO

Trailing 12 months

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

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