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EA STIMULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080221
510(k) Type
Traditional
Applicant
HELIO MEDICAL SUPPLIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/2008
Days to Decision
224 days
Submission Type
Summary

EA STIMULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080221
510(k) Type
Traditional
Applicant
HELIO MEDICAL SUPPLIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/2008
Days to Decision
224 days
Submission Type
Summary