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HYPERTHERMIA PUMP

Page Type
Cleared 510(K)
510(k) Number
K070654
510(k) Type
Traditional
Applicant
BELMONT INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/2007
Days to Decision
91 days
Submission Type
Summary

HYPERTHERMIA PUMP

Page Type
Cleared 510(K)
510(k) Number
K070654
510(k) Type
Traditional
Applicant
BELMONT INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/2007
Days to Decision
91 days
Submission Type
Summary