510(k) K771694
K771694 is an FDA 510(k) premarket notification submitted by Terumo America, Inc. for the device "CLIRANS TH 15 HOLLOW FIBER DIALYZER". The FDA issued a decision of Substantially Equivalent on September 15, 1977. The device falls under product code FJI (Dialyzer, Capillary, Hollow Fiber), a Class II device regulated under 21 CFR 876.5820. Terumo America, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 15, 1977
- Date Received
- September 6, 1977
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Dialyzer, Capillary, Hollow Fiber
- Device Class
- Class II
- Regulation Number
- 876.5820
- Review Panel
- GU
- Submission Type