ClearanceBrief
Company ยท US

Vee Gee Scientific, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1994 to 1995. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
JRERefractometer For Clinical Use6

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jan 17, 1995K941906MODEL 2730 CLINICAL REFRACTOMETER
Vee Gee Scientific, Inc.
JRE
Jan 17, 1995K941903MODEL 2740 CLINICAL REFRACTOMETER
Vee Gee Scientific, Inc.
JRE
Jan 17, 1995K941901MODEL 2721 CLINICAL REFRACTOMETER
Vee Gee Scientific, Inc.
JRE
Dec 13, 1994K941905MODEL 3461 CLINICAL REFRACTOMETER
Vee Gee Scientific, Inc.
JRE
Dec 13, 1994K941904MODEL A300CL CLINICAL REFRACTOMETER
Vee Gee Scientific, Inc.
JRE
Dec 13, 1994K941902MODEL 3471 CLINICAL REFRACTOMETER
Vee Gee Scientific, Inc.
JRE

Latest recalls

DateFirm and productCodeLinked 510(k)
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