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TERUMO ANGIOGRAPHIC CATHETER FOR LAPOROSCOPIC USE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K926217
510(k) Type
Traditional
Applicant
TERUMO MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/1993
Days to Decision
215 days
Submission Type
Statement

TERUMO ANGIOGRAPHIC CATHETER FOR LAPOROSCOPIC USE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K926217
510(k) Type
Traditional
Applicant
TERUMO MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/1993
Days to Decision
215 days
Submission Type
Statement