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DREAMGARD REM-SOFT, DREAMGARD REM-LITE, DREAMGARD REM-ULTRA, DREAMGARD REM-MAX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112868
510(k) Type
Traditional
Applicant
DREAMGARD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2012
Days to Decision
111 days
Submission Type
Summary

DREAMGARD REM-SOFT, DREAMGARD REM-LITE, DREAMGARD REM-ULTRA, DREAMGARD REM-MAX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112868
510(k) Type
Traditional
Applicant
DREAMGARD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2012
Days to Decision
111 days
Submission Type
Summary