CODMAN GAAB NEUROENDOSCOPE— 510(k) K923555
Substantially EquivalentCodman & Shurtleff, Inc.
FDA 510(k) clearance K923555 for CODMAN GAAB NEUROENDOSCOPE, Substantially Equivalent on 1993-03-23. Applicant: Codman & Shurtleff, Inc.. Device class: 1.
Clearance details
- Applicant
- Codman & Shurtleff, Inc.
- Product code
- Code GWB
- Device class
- Class 1
- Regulation
- 21 CFR 866.3740
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Randolph, MA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.