Last synced on 25 January 2026 at 3:41 am

EMBRYON SINGLE AND DOUBLE LUMEN NEEDLES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000205
510(k) Type
Traditional
Applicant
Rocket Medical Plc
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
4/19/2000
Days to Decision
89 days
Submission Type
Summary

EMBRYON SINGLE AND DOUBLE LUMEN NEEDLES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000205
510(k) Type
Traditional
Applicant
Rocket Medical Plc
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
4/19/2000
Days to Decision
89 days
Submission Type
Summary