510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K981163Substantially Equivalent

Diamedix Is-Cmv Igg Test System

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

K981163 is the FDA 510(k) clearance record for DIAMEDIX IS-CMV IGG TEST SYSTEM, a class II device, cleared for Diamedix Corp. on under FDA product code LFZ (Enzyme Linked Immunoabsorbent Assay, Cytomegalovirus). FDA records list 68 510(k) clearances for Diamedix Corp., from to . As of , FDA records show one recall naming K981163.

Clearance record

Decision date
Received
(174 days to decision)
Product code
LFZ Enzyme Linked Immunoabsorbent Assay, Cytomegalovirus
Regulation
21 CFR 866.3175
Device class
Class II
Review panel
Microbiology
Applicant
Diamedix Corp. 2140 N. Miami Ave., Miami FL
510(k) summary
Summary
Third party review
No

Clearances, product code LFZ

Trailing 12 months

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

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