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OGDEN ANCHOR (MODIFICATION)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K935167
510(k) Type
Traditional
Applicant
AMERICAN MEDICAL ELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
7/12/1994
Days to Decision
258 days
Submission Type
Summary

OGDEN ANCHOR (MODIFICATION)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K935167
510(k) Type
Traditional
Applicant
AMERICAN MEDICAL ELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
7/12/1994
Days to Decision
258 days
Submission Type
Summary