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

BIO-MEDICUS BIO CONSOLE MODELS 540 A B C

K Number: K901584 · Decision Jun 28, 1990
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
36
Applicant Total
15
Review Days
85

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Basic Information

Device Name
BIO-MEDICUS BIO CONSOLE MODELS 540 A B C
K Number
K901584
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4380
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Bio Medicus, Inc.
Date Received
April 4, 1990
Decision Date
June 28, 1990
Product Code
DWA
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
DWA Control, Pump Speed, Cardiopulmonary Bypass

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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
K894980 BIO-CAL 370 HEATER/COOLER
K884129 BIO-MEDICUS PERCUTANEOUS CANNULA & INTRODUCER SET
K883956 BIO-MEDICUS TUBING CONNECTORS
K872033 BIO-MEDICUS CANNULA-TUBING
K861096 CARDIOPULMONARY CANNULA TUBING
K854133 BIO MEDICUS BIO CONSOLE 540
K853126 BIO PACK MODEL 200
Search all 15 clearances from Bio Medicus, Inc. →