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NERVE FIBER ANALYZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K941705
510(k) Type
Traditional
Applicant
CARLZEISS MEDITEC INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/1994
Days to Decision
103 days
Submission Type
Summary

NERVE FIBER ANALYZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K941705
510(k) Type
Traditional
Applicant
CARLZEISS MEDITEC INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/1994
Days to Decision
103 days
Submission Type
Summary