Last synced on 2 May 2025 at 11:05 pm

TERRAQUANT MQ2000 LASER THERAPY DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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