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CODMAN NEUROLASE LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K872179
510(k) Type
Traditional
Applicant
Codman & Shurtleff, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/1987
Days to Decision
121 days

CODMAN NEUROLASE LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K872179
510(k) Type
Traditional
Applicant
Codman & Shurtleff, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/1987
Days to Decision
121 days