STRAIGHT-LINE FINISH FOR IMPLANTABLE PULSE GENERA.— 510(k) K881749
Substantially EquivalentMedtronic Vascular
FDA 510(k) clearance K881749 for STRAIGHT-LINE FINISH FOR IMPLANTABLE PULSE GENERA., Substantially Equivalent on 1988-07-18. Applicant: Medtronic Vascular. Device class: 2.
Clearance details
- Applicant
- Medtronic Vascular
- Product code
- Code GXY
- Device class
- Class 2
- Regulation
- 21 CFR 882.1320
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Minneapolis, MN, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.