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EUP-V12 5.0 MHZ CONVEX ARRAY TRANSVAGINAL PROBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900966
510(k) Type
Traditional
Applicant
HITACHI MEDICAL CORP. OF AMERICA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/1990
Days to Decision
195 days

EUP-V12 5.0 MHZ CONVEX ARRAY TRANSVAGINAL PROBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900966
510(k) Type
Traditional
Applicant
HITACHI MEDICAL CORP. OF AMERICA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/1990
Days to Decision
195 days