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

FDA Device Classification

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