Last synced on 18 April 2025 at 11:05 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

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