Last synced on 19 July 2024 at 11:05 pm

PROMAX-XP, TENS AND MICROCURRENT DEVICE; PROMAX-TENS, TENS DEVICE; PROMAX-LIBRA, TENS DEVICE; PROMAX-MC, MICROCURRENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011017
510(k) Type
Traditional
Applicant
REHABILICARE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/24/2001
Days to Decision
173 days
Submission Type
Summary

PROMAX-XP, TENS AND MICROCURRENT DEVICE; PROMAX-TENS, TENS DEVICE; PROMAX-LIBRA, TENS DEVICE; PROMAX-MC, MICROCURRENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011017
510(k) Type
Traditional
Applicant
REHABILICARE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/24/2001
Days to Decision
173 days
Submission Type
Summary