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PHILIPS INTEGRIS V3000 ROTATIONAL ANGIO FUNCTION

Page Type
Cleared 510(K)
510(k) Number
K923813
510(k) Type
Traditional
Applicant
PHILIPS MEDICAL SYSTEMS, INC.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
10/16/1992
Days to Decision
79 days
Submission Type
Summary

PHILIPS INTEGRIS V3000 ROTATIONAL ANGIO FUNCTION

Page Type
Cleared 510(K)
510(k) Number
K923813
510(k) Type
Traditional
Applicant
PHILIPS MEDICAL SYSTEMS, INC.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
10/16/1992
Days to Decision
79 days
Submission Type
Summary