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ANNULAR ARRAY PROBES FOR ARTIS 3200 DIAG. ULTRA.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881185
510(k) Type
Traditional
Applicant
PHILIPS MEDICAL SYSTEMS(CLEVELAND), INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/1988
Days to Decision
72 days

ANNULAR ARRAY PROBES FOR ARTIS 3200 DIAG. ULTRA.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881185
510(k) Type
Traditional
Applicant
PHILIPS MEDICAL SYSTEMS(CLEVELAND), INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/1988
Days to Decision
72 days