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

BIO MEDICUS BIO PUMP MODEL BP-80

K Number: K852698 · Decision Sep 30, 1985
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
83
Applicant Total
15
Review Days
96

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Basic Information

Device Name
BIO MEDICUS BIO PUMP MODEL BP-80
K Number
K852698
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4360
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Bio Medicus, Inc.
Date Received
June 26, 1985
Decision Date
September 30, 1985
Product Code
KFM
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
KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type

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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
K861096 CARDIOPULMONARY CANNULA TUBING
K854133 BIO MEDICUS BIO CONSOLE 540
Search all 15 clearances from Bio Medicus, Inc. →