Last synced on 25 January 2026 at 3:41 am

MEDIFIX INC.

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992483
510(k) Type
Traditional
Applicant
Medifix, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/1999
Days to Decision
35 days
Submission Type
Summary

MEDIFIX INC.

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992483
510(k) Type
Traditional
Applicant
Medifix, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/1999
Days to Decision
35 days
Submission Type
Summary