CODMAN STEERABLE ENDOSCOPE (CAT.# 83-1340)— 510(k) K920979
Substantially EquivalentCodman & Shurtleff, Inc.
FDA 510(k) clearance K920979 for CODMAN STEERABLE ENDOSCOPE (CAT.# 83-1340), Substantially Equivalent on 1993-03-23. Applicant: Codman & Shurtleff, Inc.. Device class: 2.
Clearance details
- Applicant
- Codman & Shurtleff, Inc.
- Product code
- Code GCQ
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Attleboro, MA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.