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

THE BELMONT BUDDY LITE FLUID WARMER

K Number: K112639 · Decision Nov 16, 2011
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
13
Applicant Total
20
Review Days
65

Basic Information

Device Name
THE BELMONT BUDDY LITE FLUID WARMER
K Number
K112639
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
864.9205
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
BELMONT INSTRUMENT CORP.
Date Received
September 12, 2011
Decision Date
November 16, 2011
Product Code
BSB
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
BSB Warmer, Blood, Non-Electromagnetic Radiation

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Other Clearances by BELMONT INSTRUMENT CORP.

K Number Device Name
K131519 BELMONT HYPERTHERMIA PUMP
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
K031478 MICROHEATER
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