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Truscope Ultra Patient Monitor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162234
510(k) Type
Special
Applicant
GUANGDONG BIOLIGHT MEDITECH CO., LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
1/4/2017
Days to Decision
148 days
Submission Type
Statement

Truscope Ultra Patient Monitor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162234
510(k) Type
Special
Applicant
GUANGDONG BIOLIGHT MEDITECH CO., LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
1/4/2017
Days to Decision
148 days
Submission Type
Statement