Last synced on 2 December 2022 at 11:04 pm

ENOLOK-FOR ENDOSCOPED WITH 12.8>DIA.<13.3MM SHAFT DIAMETER, MODEL AEL; ENDOSCOPES WITH 11.3>DIA. 11.5MM SHAFT ,MODEL PEL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080317
510(k) Type
Traditional
Applicant
SYNTHEON LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/2008
Days to Decision
83 days
Submission Type
Summary

ENOLOK-FOR ENDOSCOPED WITH 12.8>DIA.<13.3MM SHAFT DIAMETER, MODEL AEL; ENDOSCOPES WITH 11.3>DIA. 11.5MM SHAFT ,MODEL PEL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080317
510(k) Type
Traditional
Applicant
SYNTHEON LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/2008
Days to Decision
83 days
Submission Type
Summary