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

BELMONT HYPERTHERMIA PUMP

K Number: K090089 · Decision Feb 12, 2009
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
74
Applicant Total
20
Review Days
29

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Basic Information

Device Name
BELMONT HYPERTHERMIA PUMP
K Number
K090089
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Belmont Instrument Corp.
Date Received
January 14, 2009
Decision Date
February 12, 2009
Product Code
LGZ
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LGZ Warmer, Thermal, Infusion Fluid

Similar 510(k) Clearances

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

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Other Clearances by Belmont Instrument Corp.

K Number Device Name
K131519 BELMONT HYPERTHERMIA PUMP
K112639 THE BELMONT BUDDY LITE FLUID WARMER
K091855 THE BELMONT FLUID MANAGEMENT SYSTEM/ THE BELMONT RAPID INFUSER, MODEL FMS2000
K090508 THE BELMONT BUDDY LITE FLUID WARMER
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
K031478 MICROHEATER
Search all 20 clearances from Belmont Instrument Corp. →