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MAYFIELD* A-2000 SKULL CLAMP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932807
510(k) Type
Traditional
Applicant
OHIO MEDICAL INSTRUMENT CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/1993
Days to Decision
111 days
Submission Type
Summary

MAYFIELD* A-2000 SKULL CLAMP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932807
510(k) Type
Traditional
Applicant
OHIO MEDICAL INSTRUMENT CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/1993
Days to Decision
111 days
Submission Type
Summary