Last synced on 11 July 2025 at 11:06 pm

DYNAPHOR(TM) 101, IONTOPHORESIS DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K894549
510(k) Type
Traditional
Applicant
HENLEY INTL.
Country
United States
FDA Decision
Substantially Equivalent with Drug
Decision Date
2/9/1990
Days to Decision
204 days

DYNAPHOR(TM) 101, IONTOPHORESIS DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K894549
510(k) Type
Traditional
Applicant
HENLEY INTL.
Country
United States
FDA Decision
Substantially Equivalent with Drug
Decision Date
2/9/1990
Days to Decision
204 days