DESERET SUBCLAVIAN HEMODIALYSIS CATHETER— 510(k) K881695
Substantially EquivalentDeseret Medical, Inc.
FDA 510(k) clearance K881695 for DESERET SUBCLAVIAN HEMODIALYSIS CATHETER, Substantially Equivalent on 1988-06-23. Applicant: Deseret Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Deseret Medical, Inc.
- Product code
- Code LFJ
- Device class
- Class 2
- Regulation
- 21 CFR 876.5540
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Sandy, UT, US
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