COMBIPORT FLUID LAVAGE DEVICE— 510(k) K971259
Substantially EquivalentB.Braun Medical, Inc.
FDA 510(k) clearance K971259 for COMBIPORT FLUID LAVAGE DEVICE, Substantially Equivalent on 1997-10-27. Applicant: B.Braun Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- B.Braun Medical, Inc.
- Product code
- Code KDH
- Device class
- Class 2
- Regulation
- 21 CFR 876.5980
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Allentown, PA, US
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