DEMIPULSE MODEL 103 GENERATOR AND ASPIRESR MODEL 106 GENERATOR
FDA premarket approval P970003/S180 · decided 2015-07-08
Approval details
- PMA number
- P970003
- Supplement
- S180
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- DEMIPULSE MODEL 103 GENERATOR AND ASPIRESR MODEL 106 GENERATOR
- Generic name
- Stimulator, autonomic nerve, implanted (depression)
- Applicant
- LivaNova USA, Inc.
- Date received
- 2015-06-08
- Decision date
- 2015-07-08
- Days to decision
- 30 days
- Decision code
- OK30
- Product code
- MUZ
- Advisory committee
- Neurology
- Expedited review
- No
- Location
- Houston, TX
- Statement
- USE OF AN ALTERNATE ELECTRICAL TEST SYSTEM (ETS) KNOWN AS THE UNIVERSAL TEST SYSTEM (UTS) FOR THE MODEL 106 GENERATOR.
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