Last synced on 2 December 2022 at 11:04 pm

COAPTITE LARYNGEAL AUGMENTATION SYSTEM 1CC & O.5CC, MODELS 0008021-1, 0008022-1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013243
510(k) Type
Traditional
Applicant
BIOFORM, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2002
Days to Decision
103 days
Submission Type
Summary

COAPTITE LARYNGEAL AUGMENTATION SYSTEM 1CC & O.5CC, MODELS 0008021-1, 0008022-1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013243
510(k) Type
Traditional
Applicant
BIOFORM, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2002
Days to Decision
103 days
Submission Type
Summary