Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K121752Substantially Equivalent

Avie Total Hb Test System

Mec Dynamics Corp, San Jose CA / Traditional, Substantially Equivalent

K121752 is the FDA 510(k) clearance record for AVIE TOTAL HB TEST SYSTEM, a class II device, cleared for Mec Dynamics Corp on under FDA product code GKR (System, Hemoglobin, Automated). FDA records list 4 510(k) clearances for Mec Dynamics Corp, from to . As of , FDA records show no recalls naming K121752.

Clearance record

Decision date
Received
(207 days to decision)
Product code
GKR System, Hemoglobin, Automated
Regulation
21 CFR 864.5620
Device class
Class II
Review panel
Hematology
Applicant
Mec Dynamics Corp 90 Rose Orchard Way, San Jose CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GKR

Trailing 12 months

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

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