Product code GWB— Microbiology
CODMAN GAAB NEUROENDOSCOPE
- Classification name
- Antisera, Fluorescent, All Types, Streptococcus Pneumoniae
- Device class
- Class 1
- Regulation
- 21 CFR 866.3740
- Advisory panel
- Microbiology
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code GWB
FDA has cleared devices under product code GWB between 1976 and 1993, filed by 2 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 1993
- 1976
Top applicants under product code GWB
Recent clearances under product code GWB
Data sourced from openFDA. This site is unofficial and independent of the FDA.