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RELIEFBAND NST DEVICE MODELS WB-2,WB-6,WB-R

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983907
510(k) Type
Traditional
Applicant
WOODSIDE BIOMEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/1999
Days to Decision
401 days
Submission Type
Statement

RELIEFBAND NST DEVICE MODELS WB-2,WB-6,WB-R

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983907
510(k) Type
Traditional
Applicant
WOODSIDE BIOMEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/1999
Days to Decision
401 days
Submission Type
Statement