510(k) K791846
K791846 is an FDA 510(k) premarket notification submitted by Dlp, Inc. for the device "DISPOSSABLE SUCTION TUBE, 6 FRENCH". The FDA issued a decision of Substantially Equivalent on October 2, 1979. The device falls under product code DTS (Sucker, Cardiotomy Return, Cardiopulmonary Bypass), a Class II device regulated under 21 CFR 870.4420. Dlp, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 2, 1979
- Date Received
- September 19, 1979
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Sucker, Cardiotomy Return, Cardiopulmonary Bypass
- Device Class
- Class II
- Regulation Number
- 870.4420
- Review Panel
- CV
- Submission Type