510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K013628Substantially Equivalent

Diamedix Is-Anti-B2 Glycoprotein I Igg/igm Test System

Diamedix Corp., Miami FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K013628 is the FDA 510(k) clearance record for DIAMEDIX IS-ANTI-B2 GLYCOPROTEIN I IGG/IGM TEST SYSTEM, a class II device, cleared for Diamedix Corp. on under FDA product code MSV (System,Test,Antibodies,B2 - Glycoprotein I (B2 - Gpi)). FDA records list 68 510(k) clearances for Diamedix Corp., from to . As of , FDA records show no recalls naming K013628.

Clearance record

Decision date
Received
(46 days to decision)
Product code
MSV System,Test,Antibodies,B2 - Glycoprotein I (B2 - Gpi)
Regulation
21 CFR 866.5660
Device class
Class II
Review panel
Immunology
Applicant
Diamedix Corp. 2140 N. Miami Ave., Miami FL
510(k) summary
Summary
Third party review
No

Clearances, product code MSV

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