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RELIEFBAND NST DEVICE, MODEL WB-2L, WB-6L, WB-RL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K994387
510(k) Type
Traditional
Applicant
WOODSIDE BIOMEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/2000
Days to Decision
79 days
Submission Type
Summary

RELIEFBAND NST DEVICE, MODEL WB-2L, WB-6L, WB-RL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K994387
510(k) Type
Traditional
Applicant
WOODSIDE BIOMEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/2000
Days to Decision
79 days
Submission Type
Summary