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

SARNS TURBO MEMBRANE OXYGENATOR MODIFICATION

K Number: K941653 · Decision Aug 24, 1994
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
249
Applicant Total
76
Review Days
141

Basic Information

Device Name
SARNS TURBO MEMBRANE OXYGENATOR MODIFICATION
K Number
K941653
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4350
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
3M HEALTH CARE, SARNS
Date Received
April 5, 1994
Decision Date
August 24, 1994
Product Code
DTZ
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
DTZ Oxygenator, Cardiopulmonary Bypass

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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
K925076 SARNS TURBO MEMBRANE OXYGENA. W/INT. CARDIOTOMY R.
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