Last synced on 25 January 2026 at 3:41 am

FINGERTIP PULSE OXIMETER, MODEL M70, AND HANDHELD PULSE OXIMETER, MODEL M700

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081712
510(k) Type
Traditional
Applicant
Guangdong Biolight Meditech Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
9/12/2008
Days to Decision
87 days
Submission Type
Summary

FINGERTIP PULSE OXIMETER, MODEL M70, AND HANDHELD PULSE OXIMETER, MODEL M700

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081712
510(k) Type
Traditional
Applicant
Guangdong Biolight Meditech Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
9/12/2008
Days to Decision
87 days
Submission Type
Summary