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EPILASER I UPGRADE KIT

Page Type
Cleared 510(K)
510(k) Number
K980160
510(k) Type
Traditional
Applicant
PALOMAR MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/1998
Days to Decision
53 days
Submission Type
Summary

EPILASER I UPGRADE KIT

Page Type
Cleared 510(K)
510(k) Number
K980160
510(k) Type
Traditional
Applicant
PALOMAR MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/10/1998
Days to Decision
53 days
Submission Type
Summary