PULSE GENERATOR MODEL 61 AND 128
FDA 510(k) clearance K790562 · decided 1979-05-08
Clearance details
- K-number
- K790562
- Device name
- PULSE GENERATOR MODEL 61 AND 128
- Applicant
- Ela Medical, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1979-03-19
- Decision date
- 1979-05-08
- Days to decision
- 50 days
- Clearance type
- Traditional
- Product code
- DXY
- Device class
- 3
- Regulation number
- 870.3610
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
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Recalls involving this device
No recalls on record reference this clearance.