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INTRAUTERINE INSEMINATION AND SONOHYSTEROGRAPHY CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970492
510(k) Type
Traditional
Applicant
ACKRAD LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/1997
Days to Decision
58 days
Submission Type
Summary

INTRAUTERINE INSEMINATION AND SONOHYSTEROGRAPHY CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970492
510(k) Type
Traditional
Applicant
ACKRAD LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/1997
Days to Decision
58 days
Submission Type
Summary