ENDOSCOPIC RETROGRADE— 510(k) K833417
Substantially EquivalentMicrovasive
FDA 510(k) clearance K833417 for ENDOSCOPIC RETROGRADE, Substantially Equivalent on 1983-11-28. Applicant: Microvasive. Device class: 2.
Clearance details
- Applicant
- Microvasive
- Product code
- Code ODD
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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More clearances from Microvasive
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