Last synced on 27 May 2022 at 11:05 pm

Y2000 MANUAL RESUSCITATOR, MODEL RUGU01/RUG02 AND RUGH01/RUGH02

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003927
510(k) Type
Traditional
Applicant
CHEEN HOUNG ENT. CO. LTD.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
6/26/2001
Days to Decision
188 days
Submission Type
Summary

Y2000 MANUAL RESUSCITATOR, MODEL RUGU01/RUG02 AND RUGH01/RUGH02

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003927
510(k) Type
Traditional
Applicant
CHEEN HOUNG ENT. CO. LTD.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
6/26/2001
Days to Decision
188 days
Submission Type
Summary