PERI-PATCH PERITONEAL CATHETER EXTENSION— 510(k) K810531
Substantially EquivalentQuinton, Inc.
FDA 510(k) clearance K810531 for PERI-PATCH PERITONEAL CATHETER EXTENSION, Substantially Equivalent on 1981-03-24. Applicant: Quinton, Inc.. Device class: 1.
Clearance details
- Applicant
- Quinton, Inc.
- Product code
- Code KGZ
- 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
- Mchenry, IL, US
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