510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K925210Substantially Equivalent

90Dx Multitest Meter, Modification

Mesa Medical, Inc., Wheat Ridge CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K925210 is the FDA 510(k) clearance record for 90DX MULTITEST METER, MODIFICATION, a class II device, cleared for Mesa Medical, Inc. on under FDA product code FLB (Meter, Conductivity, Induction, Remote Type). FDA records list 7 510(k) clearances for Mesa Medical, Inc., from to . As of , FDA records show no recalls naming K925210.

Clearance record

Decision date
Received
(475 days to decision)
Product code
FLB Meter, Conductivity, Induction, Remote Type
Regulation
21 CFR 876.5820
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Mesa Medical, Inc. 3904 Youngfield St., Wheat Ridge CO
510(k) summary
Summary
Third party review
No

Clearances, product code FLB

Trailing 12 months

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

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