Last synced on 23 September 2022 at 11:05 pm

AV 800 VENTILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010317
510(k) Type
Traditional
Applicant
PENLON LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
7/23/2001
Days to Decision
171 days
Submission Type
Summary

AV 800 VENTILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010317
510(k) Type
Traditional
Applicant
PENLON LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
7/23/2001
Days to Decision
171 days
Submission Type
Summary