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ALLURA 3D-CA, RELEASE 1

Page Type
Cleared 510(K)
510(k) Number
K042334
510(k) Type
Traditional
Applicant
Philips Medical Systems North America Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/2004
Days to Decision
28 days
Submission Type
Summary

ALLURA 3D-CA, RELEASE 1

Page Type
Cleared 510(K)
510(k) Number
K042334
510(k) Type
Traditional
Applicant
Philips Medical Systems North America Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/2004
Days to Decision
28 days
Submission Type
Summary