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EPIDURAL CATHETER MODELS 1210/1200

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983125
510(k) Type
Traditional
Applicant
RUSCH INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/1998
Days to Decision
70 days
Submission Type
Summary

EPIDURAL CATHETER MODELS 1210/1200

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983125
510(k) Type
Traditional
Applicant
RUSCH INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/1998
Days to Decision
70 days
Submission Type
Summary