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KENEX INJECTOR HEAD SUPPORT (AS EXHIBIT 2)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K951005
510(k) Type
Traditional
Applicant
KENEX LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
5/4/1995
Days to Decision
78 days
Submission Type
Summary

KENEX INJECTOR HEAD SUPPORT (AS EXHIBIT 2)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K951005
510(k) Type
Traditional
Applicant
KENEX LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
5/4/1995
Days to Decision
78 days
Submission Type
Summary