CATHETER, MULTIPLE LUMEN— 510(k) K820446
Substantially EquivalentDlp, Inc.
FDA 510(k) clearance K820446 for CATHETER, MULTIPLE LUMEN, Substantially Equivalent on 1982-03-11. Applicant: Dlp, Inc.. Device class: 1.
Clearance details
- Applicant
- Dlp, Inc.
- Product code
- Code GBP
- Device class
- Class 1
- Regulation
- 21 CFR 878.4200
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
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