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INJECTION NEEDLE PROBE/DEVICE-TUNIS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983765
510(k) Type
Traditional
Applicant
XIMED/PROSURE/INJECTX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/1998
Days to Decision
46 days
Submission Type
Statement

INJECTION NEEDLE PROBE/DEVICE-TUNIS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983765
510(k) Type
Traditional
Applicant
XIMED/PROSURE/INJECTX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/1998
Days to Decision
46 days
Submission Type
Statement