QUICVAGE— 510(k) K914907
Substantially EquivalentAutovage
FDA 510(k) clearance K914907 for QUICVAGE, Substantially Equivalent on 1992-01-24. Applicant: Autovage. Device class: 2.
Clearance details
- Applicant
- Autovage
- Product code
- Code KDH
- Device class
- Class 2
- Regulation
- 21 CFR 876.5980
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- South Park, PA, US
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