510(k) K852232

PRESSURE DISPLAY BOX #60000/TUBING SET #61000 by Dlp, Inc. — Product Code DXS

K852232 is an FDA 510(k) premarket notification submitted by Dlp, Inc. for the device "PRESSURE DISPLAY BOX #60000/TUBING SET #61000". The FDA issued a decision of Substantially Equivalent on August 9, 1985. The device falls under product code DXS (Gauge, Pressure, Coronary, Cardiopulmonary Bypass), a Class II device regulated under 21 CFR 870.4310. Dlp, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 9, 1985
Date Received
May 22, 1985
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