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
K941903Substantially Equivalent

Model 2740 Clinical Refractometer

Vee Gee Scientific, Inc., Kirkland WA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K941903 is the FDA 510(k) clearance record for MODEL 2740 CLINICAL REFRACTOMETER, a class I device, cleared for Vee Gee Scientific, Inc. on under FDA product code JRE (Refractometer For Clinical Use). FDA records list 6 510(k) clearances for Vee Gee Scientific, Inc., from to . As of , FDA records show no recalls naming K941903.

Clearance record

Decision date
Received
(273 days to decision)
Product code
JRE Refractometer For Clinical Use
Regulation
21 CFR 862.2800
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Vee Gee Scientific, Inc. 13600 NE 126th Pl., Suite A, Kirkland WA
510(k) summary
Summary
Third party review
No

Clearances, product code JRE

Trailing 12 months

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

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