Last synced on 30 September 2022 at 11:05 pm

FETAL MONITORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131941
510(k) Type
Traditional
Applicant
GUANGDONG BIOLIGHT MEDITECH CO., LTD
Country
China
FDA Decision
Substantially Equivalent
Decision Date
5/15/2014
Days to Decision
322 days
Submission Type
Summary

FETAL MONITORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131941
510(k) Type
Traditional
Applicant
GUANGDONG BIOLIGHT MEDITECH CO., LTD
Country
China
FDA Decision
Substantially Equivalent
Decision Date
5/15/2014
Days to Decision
322 days
Submission Type
Summary