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GEMINI SURGICAL LIGHT

Page Type
Cleared 510(K)
510(k) Number
K880198
510(k) Type
Traditional
Applicant
AMERICAN STERILIZER CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1988
Days to Decision
26 days

GEMINI SURGICAL LIGHT

Page Type
Cleared 510(K)
510(k) Number
K880198
510(k) Type
Traditional
Applicant
AMERICAN STERILIZER CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1988
Days to Decision
26 days