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RELIEFBAND NST DEVICE, MODEL #'S WB-2, WB-6 AND WB-R

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982436
510(k) Type
Traditional
Applicant
WOODSIDE BIOMEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/1998
Days to Decision
86 days
Submission Type
Summary

RELIEFBAND NST DEVICE, MODEL #'S WB-2, WB-6 AND WB-R

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982436
510(k) Type
Traditional
Applicant
WOODSIDE BIOMEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/1998
Days to Decision
86 days
Submission Type
Summary