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

EXTERNAL HELIUM SUPPLY (ACCESSORY FOR IABP)

K Number: K950687 · Decision May 24, 1995
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
161
Applicant Total
20
Review Days
99

Basic Information

Device Name
EXTERNAL HELIUM SUPPLY (ACCESSORY FOR IABP)
K Number
K950687
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.3535
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
BELMONT INSTRUMENT CORP.
Date Received
February 14, 1995
Decision Date
May 24, 1995
Product Code
DSP
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
DSP System, Balloon, Intra-Aortic And Control

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Other Clearances by BELMONT INSTRUMENT CORP.

K Number Device Name
K131519 BELMONT HYPERTHERMIA PUMP
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K091855 THE BELMONT FLUID MANAGEMENT SYSTEM/ THE BELMONT RAPID INFUSER, MODEL FMS2000
K090508 THE BELMONT BUDDY LITE FLUID WARMER
K090089 BELMONT HYPERTHERMIA PUMP
K070654 HYPERTHERMIA PUMP
K062774 BELMONT BUDDY PLUS FLUID WARMER
K052547 BELMONT BUDDY FLUID WARMER
K032778 LARGE VOLUME FLUID RESERVOIR
K032674 BELMONT FLUID MANAGEMENT SYSTEM, MODEL FMS2000
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