Last synced on 19 July 2024 at 11:05 pm

DYNEX III TRANSCUTANEOUS ELECTRICAL NERVE STIMULA.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K864956
510(k) Type
Traditional
Applicant
LA JOLLA TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/9/1987
Days to Decision
81 days

DYNEX III TRANSCUTANEOUS ELECTRICAL NERVE STIMULA.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K864956
510(k) Type
Traditional
Applicant
LA JOLLA TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/9/1987
Days to Decision
81 days