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PHILIPS ANGIOPRO RELEASE 2.1

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K933791
510(k) Type
Traditional
Applicant
PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/1993
Days to Decision
110 days
Submission Type
Summary

PHILIPS ANGIOPRO RELEASE 2.1

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K933791
510(k) Type
Traditional
Applicant
PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/1993
Days to Decision
110 days
Submission Type
Summary