VA 1000— 510(k) K791380
Substantially EquivalentVitatron Medical BV
FDA 510(k) clearance K791380 for VA 1000, Substantially Equivalent on 1979-09-19. Applicant: Vitatron Medical BV. Device class: 2.
Clearance details
- Applicant
- Vitatron Medical BV
- Product code
- Code DTA
- Device class
- Class 2
- Regulation
- 21 CFR 870.3720
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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