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DIOMED 25 SURGICAL DIODE LASER, GYNECOLOGY APPLIC

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914519
510(k) Type
Traditional
Applicant
DIO-MED CORP.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
9/16/1993
Days to Decision
707 days
Submission Type
Summary

DIOMED 25 SURGICAL DIODE LASER, GYNECOLOGY APPLIC

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914519
510(k) Type
Traditional
Applicant
DIO-MED CORP.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
9/16/1993
Days to Decision
707 days
Submission Type
Summary