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KENDALL BLUNT TUOHY EPIDURAL NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K954706
510(k) Type
Traditional
Applicant
KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH
Country
United States
FDA Decision
Substantially Equivalent with Drug
Decision Date
5/30/1996
Days to Decision
231 days
Submission Type
Summary

KENDALL BLUNT TUOHY EPIDURAL NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K954706
510(k) Type
Traditional
Applicant
KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH
Country
United States
FDA Decision
Substantially Equivalent with Drug
Decision Date
5/30/1996
Days to Decision
231 days
Submission Type
Summary