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

BIO-PROBE SYSTEM-BLOOD FLOW PROBE

K Number: K830858 · Decision Jun 8, 1983
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
47
Applicant Total
15
Review Days
83

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Basic Information

Device Name
BIO-PROBE SYSTEM-BLOOD FLOW PROBE
K Number
K830858
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2120
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Bio Medicus, Inc.
Date Received
March 17, 1983
Decision Date
June 8, 1983
Product Code
DPT
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
DPT Probe, Blood-Flow, Extravascular

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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. →