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TRANSVAGINAL ULTRASOUND PROBE HOLDER DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992071
510(k) Type
Traditional
Applicant
RON-TECH MEDICAL LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
8/27/1999
Days to Decision
70 days
Submission Type
Statement

TRANSVAGINAL ULTRASOUND PROBE HOLDER DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992071
510(k) Type
Traditional
Applicant
RON-TECH MEDICAL LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
8/27/1999
Days to Decision
70 days
Submission Type
Statement