510(k) K781890

CHAMBER, MC-1 DISPOSABLE PRESSURE by Delta Medical Industries — Product Code DXS

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