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HEITER 3000 HYPERTHERMIC PERFUSION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K102900
510(k) Type
Traditional
Applicant
HEI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2012
Days to Decision
538 days
Submission Type
Summary

HEITER 3000 HYPERTHERMIC PERFUSION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K102900
510(k) Type
Traditional
Applicant
HEI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2012
Days to Decision
538 days
Submission Type
Summary