CHAKOFF ENDOSCOPY— 510(k) K945421
Substantially EquivalentStephen Chakoff, Inc.
FDA 510(k) clearance K945421 for CHAKOFF ENDOSCOPY, Substantially Equivalent on 1994-12-23. Applicant: Stephen Chakoff, Inc.. Device class: 1.
Clearance details
- Applicant
- Stephen Chakoff, Inc.
- Product code
- Code FDG
- Device class
- Class 1
- Regulation
- 21 CFR 876.4530
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Miami, FL, US
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