Last synced on 14 June 2024 at 11:05 pm

HIVOX ELECTRIC STIMULATOR TENS & EMS, HD2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092448
510(k) Type
Traditional
Applicant
HIVOX BIOTEK, INC.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
3/30/2010
Days to Decision
232 days
Submission Type
Summary

HIVOX ELECTRIC STIMULATOR TENS & EMS, HD2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092448
510(k) Type
Traditional
Applicant
HIVOX BIOTEK, INC.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
3/30/2010
Days to Decision
232 days
Submission Type
Summary