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SURE-FLEX ANASTOMOTIC BALLOON DILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901433
510(k) Type
Traditional
Applicant
TELEMED SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/21/1990
Days to Decision
87 days

SURE-FLEX ANASTOMOTIC BALLOON DILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901433
510(k) Type
Traditional
Applicant
TELEMED SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/21/1990
Days to Decision
87 days