DIALYZER, FIBER, HOLLOW
FDA 510(k) clearance K770734 · decided 1977-05-10
Clearance details
- K-number
- K770734
- Device name
- DIALYZER, FIBER, HOLLOW
- Applicant
- Travenol Laboratories, S.A.
- Decision
- Substantially Equivalent
- Date received
- 1977-04-21
- Decision date
- 1977-05-10
- Days to decision
- 19 days
- Clearance type
- Traditional
- Product code
- FJI
- Device class
- 2
- Regulation number
- 876.5820
- Medical specialty
- Gastroenterology, Urology
- Advisory committee
- Gastroenterology, Urology
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.