GJW — Pipette, Pasteur Class I

FDA Device Classification

FDA product code GJW covers "Pipette, Pasteur", a Class I medical device regulated under 21 CFR 864.6160. Submissions are reviewed by the Hematology panel. At least 4 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
GJW
Device Class
Class I
Regulation Number
864.6160
Submission Type
Review Panel
HE
Medical Specialty
Hematology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K896670helena laboratoriesTIP TOP(R) DISPENSER CAPSMarch 23, 1990
K771138dade, baxter travenol diagnosticsPIPETS BOROSILICATE GLASSAugust 4, 1977
K771137dade, baxter travenol diagnosticsPIPETS UNIFORM DROP SIZE BOROSILICATEAugust 4, 1977
K760899bd becton dickinson vacutainer systems preanalyticSTERILE DISPOSABLE COTTON PLUGGED SER.November 9, 1976