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LASER LAPARAXOPE

Page Type
Cleared 510(K)
510(k) Number
K831241
510(k) Type
Traditional
Applicant
EDER INSTRUMENT CO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/1983
Days to Decision
56 days

LASER LAPARAXOPE

Page Type
Cleared 510(K)
510(k) Number
K831241
510(k) Type
Traditional
Applicant
EDER INSTRUMENT CO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/1983
Days to Decision
56 days