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

CARDIOPULMONARY CANNULA TUBING

K Number: K861096 · Decision May 21, 1986
Classifications
1
FEI Numbers
104
Registration Numbers
104
Same Product Code
400
Applicant Total
15
Review Days
58

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Basic Information

Device Name
CARDIOPULMONARY CANNULA TUBING
K Number
K861096
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4210
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Bio Medicus, Inc.
Date Received
March 24, 1986
Decision Date
May 21, 1986
Product Code
DWF
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
DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

Similar 510(k) Clearances

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

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Other Clearances by Bio Medicus, Inc.

K Number Device Name
K920761 URINE CULTUR STABILIZATION TRANSPORT TUBE
K903410 BIO-MEDICUS CANNULA INTRODUCER
K901253 (PBS) PORTABLE BYPASS SYSTEM, MODEL 1000
K901584 BIO-MEDICUS BIO CONSOLE MODELS 540 A B C
K894980 BIO-CAL 370 HEATER/COOLER
K884129 BIO-MEDICUS PERCUTANEOUS CANNULA & INTRODUCER SET
K883956 BIO-MEDICUS TUBING CONNECTORS
K872033 BIO-MEDICUS CANNULA-TUBING
K854133 BIO MEDICUS BIO CONSOLE 540
K853126 BIO PACK MODEL 200
Search all 15 clearances from Bio Medicus, Inc. →