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PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K994151
510(k) Type
Traditional
Applicant
XIMED/PROSURE/INJECTX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2000
Days to Decision
83 days
Submission Type
Statement

PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K994151
510(k) Type
Traditional
Applicant
XIMED/PROSURE/INJECTX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2000
Days to Decision
83 days
Submission Type
Statement