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LAPAROFLATOR ELECTRONIC 3509

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K910883
510(k) Type
Traditional
Applicant
F.M. WIEST USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/1991
Days to Decision
28 days

LAPAROFLATOR ELECTRONIC 3509

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K910883
510(k) Type
Traditional
Applicant
F.M. WIEST USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/1991
Days to Decision
28 days