FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SARNS PORTABLE POWER MODULE

K Number: K861388 · Decision Jun 23, 1986
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
51
Applicant Total
76
Review Days
70

Basic Information

Device Name
SARNS PORTABLE POWER MODULE
K Number
K861388
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4220
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
3M HEALTH CARE, SARNS
Date Received
April 14, 1986
Decision Date
June 23, 1986
Product Code
DTQ
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DTQ Console, Heart-Lung Machine, Cardiopulmonary Bypass

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DTQ), ordered by most recent decision date.

View all

Other Clearances by 3M HEALTH CARE, SARNS

K Number Device Name
K960916 SAMS 8000 CARDIOPLEGIA MONITOR
K953901 SARNS 800 ROLLER PUMP
K950739 3M SARNS FLOW SENSOR, CENTRIFUGAL CONTROL MODULE 115, 220 V, 900 PERFUSION SYSTEM
K941653 SARNS TURBO MEMBRANE OXYGENATOR MODIFICATION
K941654 SARNS FILTERED VENOUS RESERVIOR MODIFICATION
K940651 SARNS ULTRASONIC AIR SENSOR
K935391 SARNS STERNAL SAW II, STERNAL SAW II BLADE, SARNS SAW BLADES-NON-STERILE BULK PACK
K934127 SARNS LOW JETTING AORTIC ARCH CANNULA
K935977 SARNS AIR DETECTION SYSTEM
K915547 SARNS 8000 DELPHIN II CENTRI PUMP MOD W/INTEGR BAT
Search all 76 clearances from 3M HEALTH CARE, SARNS →