Last synced on 14 November 2025 at 11:06 pm

OPTOSCALPEL I LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K923531
510(k) Type
Traditional
Applicant
OPTOMED CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/1993
Days to Decision
484 days
Submission Type
Summary

OPTOSCALPEL I LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K923531
510(k) Type
Traditional
Applicant
OPTOMED CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/1993
Days to Decision
484 days
Submission Type
Summary