MDI 2000 - PULSE GENERATOR— 510(k) K850791
Substantially EquivalentMicromedical Devices, Inc.
FDA 510(k) clearance K850791 for MDI 2000 - PULSE GENERATOR, Substantially Equivalent on 1985-06-19. Applicant: Micromedical Devices, Inc.. Device class: 2.
Clearance details
- Applicant
- Micromedical Devices, Inc.
- Product code
- Code DRO
- Device class
- Class 2
- Regulation
- 21 CFR 870.5550
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Englewood, CO, US
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More clearances from Micromedical Devices, Inc.
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