Atlas FDA

PRESSURE DISPLAY BOX #60000/TUBING SET #61000

FDA 510(k) clearance K852232 · decided 1985-08-09

Clearance details

K-number
K852232
Device name
PRESSURE DISPLAY BOX #60000/TUBING SET #61000
Applicant
Dlp, Inc.
Decision
Substantially Equivalent
Date received
1985-05-22
Decision date
1985-08-09
Days to decision
79 days
Clearance type
Traditional
Product code
DXS
Device class
2
Regulation number
870.4310
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Grand Rapids, MI, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
PRESSURE DISPLAY BOX,DLP DISPOSABLE PRESSURE DISPLAY SETS-NON STERILE VERSIONS (K113235)Medtronic, Inc.2011-12-02
VTI DISPOSABLE PRESSURE DISPLAY SET (K944764)Vascular Technology Incorporated1994-12-27
TMP PRESSURE ISOLATORR, TMP PRESSURE MONITOR SYST (K912045)Lifestream Int'L, Inc.1991-10-31
STOCKERT SHILEY DUAL PRESSURE CONTROL MODULE XR (K900797)Shiley, Inc.1990-05-10
PRESSURE BARRIER KIT CAT. NO. PBK-3 (K873802)American Omni Medical, Inc.1987-11-06
STOCKERT-SHILEY CAPS AND CAPS DUAL PRESSURE MODULE (K862836)Shiley, Inc.1986-09-12
PRESSURE MONITOR (K842194)Norton Texas Medical Products1984-08-27
PM-3 (K831750)Delta Medical Industries1983-07-26
GAMBRO PRESSURE MONITOR PRM 10 (K822822)Gambro, Inc.1982-10-18
PMS-2 PRESSURE MONITOR SEPARATOR (K820912)Delta Medical Industries1982-05-18
CHAMBER, MC-1 DISPOSABLE PRESSURE (K781890)Delta Medical Industries1978-12-04
CORONARY PRESSURE PERFUSION PUMP (K771764)3M Health Care, Sarns1977-09-30

Recalls involving this device

RecordFirmDate
DLP Pressure Disposable Pressure Display Sets Extends the pressure line in order to reach recall (Z-2768-2017)Medtronic Perfusion Systems2017-07-10
Medtronic Pressure Display Box, Models 66000, 64000, 63000, 60000. It is capable of measur recall (Z-0077-2012)Medtronic Perfusion Systems2011-10-20
Medtronic Disposable Pressure Display Set, Models 61000, 61006, 62000, 62006. Sterilized b recall (Z-0078-2012)Medtronic Perfusion Systems2011-10-20
Medtronic Intersept Custom Tubing Pack, which are designed as specified by the user. The f recall (Z-0079-2012)Medtronic Perfusion Systems2011-10-20