510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K973177Substantially Equivalent

Mago Automated Eia Processor

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

K973177 is the FDA 510(k) clearance record for MAGO AUTOMATED EIA PROCESSOR, a class I device, cleared for Diamedix Corp. on under FDA product code JJF (Analyzer, Chemistry, Micro, For Clinical Use). FDA records list 68 510(k) clearances for Diamedix Corp., from to . As of , FDA records show no recalls naming K973177.

Clearance record

Decision date
Received
(45 days to decision)
Product code
JJF Analyzer, Chemistry, Micro, For Clinical Use
Regulation
21 CFR 862.2170
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Diamedix Corp. 2140 N. Miami Ave., Miami FL
510(k) summary
Summary
Third party review
No

Clearances, product code JJF

Trailing 12 months

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

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