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MODIFICATION TO MEDIPRIME

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023936
510(k) Type
Special
Applicant
ALGOTEC SYSTEMS, LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
12/20/2002
Days to Decision
24 days
Submission Type
Summary

MODIFICATION TO MEDIPRIME

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023936
510(k) Type
Special
Applicant
ALGOTEC SYSTEMS, LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
12/20/2002
Days to Decision
24 days
Submission Type
Summary