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TERRAQUANT MQ2000 LASER THERAPY DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043055
510(k) Type
Traditional
Applicant
Escada International, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2005
Days to Decision
262 days
Submission Type
Summary

TERRAQUANT MQ2000 LASER THERAPY DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043055
510(k) Type
Traditional
Applicant
Escada International, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2005
Days to Decision
262 days
Submission Type
Summary