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TRANSVAGINAL TRANSDUCER ASSEMBLY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900838
510(k) Type
Traditional
Applicant
PIE MEDICAL EQUIPMENT B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
5/23/1990
Days to Decision
90 days

TRANSVAGINAL TRANSDUCER ASSEMBLY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900838
510(k) Type
Traditional
Applicant
PIE MEDICAL EQUIPMENT B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
5/23/1990
Days to Decision
90 days