MODIFIED REFLUX REDUCER— 510(k) K883818
Substantially EquivalentPhysician Engineered Products, Inc.
FDA 510(k) clearance K883818 for MODIFIED REFLUX REDUCER, Substantially Equivalent on 1988-11-21. Applicant: Physician Engineered Products, Inc.. Device class: 2.
Clearance details
- Applicant
- Physician Engineered Products, Inc.
- Product code
- Code FMS
- Device class
- Class 2
- Regulation
- 21 CFR 880.5140
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Park Rapids, MN, US
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