Last synced on 12 October 2025 at 8:21 pm

DIOMED 25 SURGICAL DIODE LASER, UROLOGY APPLICAT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914520
510(k) Type
Traditional
Applicant
DIO-MED CORP.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
1/22/1993
Days to Decision
470 days
Submission Type
Statement

DIOMED 25 SURGICAL DIODE LASER, UROLOGY APPLICAT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914520
510(k) Type
Traditional
Applicant
DIO-MED CORP.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
1/22/1993
Days to Decision
470 days
Submission Type
Statement