Last synced on 14 November 2025 at 11:06 pm

DIOMED 25 SURGICAL DIODE LASER, GEN SURG APPLICAT

Page Type
Cleared 510(K)
510(k) Number
K914521
510(k) Type
Traditional
Applicant
DIO-MED CORP.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
1/15/1993
Days to Decision
463 days
Submission Type
Statement

DIOMED 25 SURGICAL DIODE LASER, GEN SURG APPLICAT

Page Type
Cleared 510(K)
510(k) Number
K914521
510(k) Type
Traditional
Applicant
DIO-MED CORP.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
1/15/1993
Days to Decision
463 days
Submission Type
Statement