CATHETER REPAIR KIT WITH REPLACEMENT CONNECTOR, MODEL 5587000— 510(k) K011015
Substantially EquivalentC.R. Bard, Inc.
FDA 510(k) clearance K011015 for CATHETER REPAIR KIT WITH REPLACEMENT CONNECTOR, MODEL 5587000, Substantially Equivalent on 2001-06-22. Applicant: C.R. Bard, Inc.. Device class: 2.
Clearance details
- Applicant
- C.R. Bard, Inc.
- Product code
- Code NFK
- Device class
- Class 2
- Regulation
- 21 CFR 876.5540
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Salt Lake City, UT, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.