510(k) K781890
K781890 is an FDA 510(k) premarket notification submitted by Delta Medical Industries for the device "CHAMBER, MC-1 DISPOSABLE PRESSURE". The FDA issued a decision of Substantially Equivalent on December 4, 1978. The device falls under product code DXS (Gauge, Pressure, Coronary, Cardiopulmonary Bypass), a Class II device regulated under 21 CFR 870.4310. Delta Medical Industries has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 4, 1978
- Date Received
- November 6, 1978
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Gauge, Pressure, Coronary, Cardiopulmonary Bypass
- Device Class
- Class II
- Regulation Number
- 870.4310
- Review Panel
- CV
- Submission Type