Last synced on 14 November 2025 at 11:06 pm

ISOLUX SURGICAL HEADLIGHT

Page Type
Cleared 510(K)
510(k) Number
K991572
510(k) Type
Traditional
Applicant
ISOLUX AMERICA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/1999
Days to Decision
64 days
Submission Type
Statement

ISOLUX SURGICAL HEADLIGHT

Page Type
Cleared 510(K)
510(k) Number
K991572
510(k) Type
Traditional
Applicant
ISOLUX AMERICA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/8/1999
Days to Decision
64 days
Submission Type
Statement