Last synced on 2 December 2022 at 11:04 pm

GUIDE WIRE FOR EDI CATHETER, 8FR,125CM,5 EACH,GUIDE WIRE FOR EDI CATHETER, 8FR,125CM,5 EACH,GUIDE WIRE FOR EDI CATHETER,

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101199
510(k) Type
Traditional
Applicant
MAQUET CRITICAL CARE AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/27/2010
Days to Decision
120 days
Submission Type
Summary