VERRES NEEDLE— 510(k) K942484
Substantially EquivalentLinvatec Corp.
FDA 510(k) clearance K942484 for VERRES NEEDLE, Substantially Equivalent on 1994-06-24. Applicant: Linvatec Corp.. Device class: 2.
Clearance details
- Applicant
- Linvatec Corp.
- Product code
- Code FHO
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Largo, FL, US
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