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MOBICATH TRANSSEPTAL NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122832
510(k) Type
Special
Applicant
Greatbatch Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/2012
Days to Decision
93 days
Submission Type
Summary

MOBICATH TRANSSEPTAL NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122832
510(k) Type
Special
Applicant
Greatbatch Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/2012
Days to Decision
93 days
Submission Type
Summary