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DIOWAVE LOW LEVEL COLD LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K121363
510(k) Type
Traditional
Applicant
TECHNOLOGICAL MEDICAL ADVANCMENTS, INC. (TMA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/2012
Days to Decision
200 days
Submission Type
Summary

DIOWAVE LOW LEVEL COLD LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K121363
510(k) Type
Traditional
Applicant
TECHNOLOGICAL MEDICAL ADVANCMENTS, INC. (TMA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/2012
Days to Decision
200 days
Submission Type
Summary