Last synced on 21 June 2024 at 11:04 pm

GIMMI ALPHA SINUSCOPES MODEL # E.8282.01/31/71 + E.8284.01/31/71; GIMMI ALPHA BRONCHOSCOPES MODEL # E.8189.00/01/02/03

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013731
510(k) Type
Traditional
Applicant
GIMMI GMBH
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
11/27/2001
Days to Decision
18 days
Submission Type
Summary

GIMMI ALPHA SINUSCOPES MODEL # E.8282.01/31/71 + E.8284.01/31/71; GIMMI ALPHA BRONCHOSCOPES MODEL # E.8189.00/01/02/03

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013731
510(k) Type
Traditional
Applicant
GIMMI GMBH
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
11/27/2001
Days to Decision
18 days
Submission Type
Summary