Last synced on 23 May 2025 at 11:06 pm

MIX2VIAL TRANSFER DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031861
510(k) Type
Traditional
Applicant
MEDIMOP MEDICAL PROJECTS, LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
7/29/2003
Days to Decision
43 days
Submission Type
Statement

MIX2VIAL TRANSFER DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031861
510(k) Type
Traditional
Applicant
MEDIMOP MEDICAL PROJECTS, LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
7/29/2003
Days to Decision
43 days
Submission Type
Statement