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

SARNS INFANT VENOUS RESERVOIR MODEL #16387

K Number: K883345 · Decision Sep 28, 1988
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
168
Applicant Total
76
Review Days
50

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Basic Information

Device Name
SARNS INFANT VENOUS RESERVOIR MODEL #16387
K Number
K883345
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4400
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
3M Health Care, Sarns
Date Received
August 9, 1988
Decision Date
September 28, 1988
Product Code
DTN
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
DTN Reservoir, Blood, Cardiopulmonary Bypass

Similar 510(k) Clearances

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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 →