Last synced on 25 January 2026 at 3:41 am

REGULUS NAVIGATOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964229
510(k) Type
Traditional
Applicant
Compass Intl., Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/1997
Days to Decision
300 days
Submission Type
Summary

REGULUS NAVIGATOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964229
510(k) Type
Traditional
Applicant
Compass Intl., Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/1997
Days to Decision
300 days
Submission Type
Summary