GWB — Antisera, Fluorescent, All Types, Streptococcus Pneumoniae Class I

FDA Device Classification

FDA product code GWB covers "Antisera, Fluorescent, All Types, Streptococcus Pneumoniae", a Class I medical device regulated under 21 CFR 866.3740. Submissions are reviewed by the Microbiology panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
GWB
Device Class
Class I
Regulation Number
866.3740
Submission Type
Review Panel
MI
Medical Specialty
Microbiology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K923555codman and shurtleffCODMAN GAAB NEUROENDOSCOPEMarch 23, 1993
K760816aftercalPNEUMOTACHOGRAPHY SYSTEMOctober 29, 1976