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AIM 200, MAJOR SURGICAL LIGHT

Page Type
Cleared 510(K)
510(k) Number
K101537
510(k) Type
Traditional
Applicant
BURTON MEDICAL PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/2010
Days to Decision
119 days
Submission Type
Summary

AIM 200, MAJOR SURGICAL LIGHT

Page Type
Cleared 510(K)
510(k) Number
K101537
510(k) Type
Traditional
Applicant
BURTON MEDICAL PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/2010
Days to Decision
119 days
Submission Type
Summary