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KELSEY INTERSITITAL LASER THERAPY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K070353
510(k) Type
Traditional
Applicant
KELSEY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2007
Days to Decision
85 days
Submission Type
Summary

KELSEY INTERSITITAL LASER THERAPY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K070353
510(k) Type
Traditional
Applicant
KELSEY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2007
Days to Decision
85 days
Submission Type
Summary