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ARTHROLUX ARTHROSCOPE

Page Type
Cleared 510(K)
510(k) Number
K821694
510(k) Type
Traditional
Applicant
ARTHRO-TECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/1982
Days to Decision
44 days

ARTHROLUX ARTHROSCOPE

Page Type
Cleared 510(K)
510(k) Number
K821694
510(k) Type
Traditional
Applicant
ARTHRO-TECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/1982
Days to Decision
44 days