Last synced on 19 July 2024 at 11:05 pm

THE MAYFIELD / ACCISS SYSTEM WITH WINDOWS NT FOR CRANIAL SURGERY, THE MAYFIELD / OPTICAL ACCISS SYSTEM WITH WINDOWS NT F

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992843
510(k) Type
Traditional
Applicant
OHIO MEDICAL INSTRUMENT CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/2/1999
Days to Decision
70 days
Submission Type
Summary

THE MAYFIELD / ACCISS SYSTEM WITH WINDOWS NT FOR CRANIAL SURGERY, THE MAYFIELD / OPTICAL ACCISS SYSTEM WITH WINDOWS NT F

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992843
510(k) Type
Traditional
Applicant
OHIO MEDICAL INSTRUMENT CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/2/1999
Days to Decision
70 days
Submission Type
Summary