PHRENIC NERVE PAD & NERVE PAD W/1/4 PERCARDIAL— 510(k) K890707
Substantially EquivalentDlp, Inc.
FDA 510(k) clearance K890707 for PHRENIC NERVE PAD & NERVE PAD W/1/4 PERCARDIAL, Substantially Equivalent on 1989-04-10. Applicant: Dlp, Inc.. Device class: 1.
Clearance details
- Applicant
- Dlp, Inc.
- Product code
- Code DWS
- Device class
- Class 1
- Regulation
- 21 CFR 870.4500
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Grand Rapids, MI, US
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