Last synced on 25 January 2026 at 3:41 am

ULTRA EASE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K950943
510(k) Type
Traditional
Applicant
Lectec Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/1996
Days to Decision
385 days
Submission Type
Summary

ULTRA EASE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K950943
510(k) Type
Traditional
Applicant
Lectec Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/1996
Days to Decision
385 days
Submission Type
Summary