Last synced on 30 May 2025 at 11:05 pm

REDSENSE-ALARM UNIT AND SENSOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103242
510(k) Type
Traditional
Applicant
REDSENSE MEDICAL AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/2011
Days to Decision
100 days
Submission Type
Summary

REDSENSE-ALARM UNIT AND SENSOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103242
510(k) Type
Traditional
Applicant
REDSENSE MEDICAL AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/2011
Days to Decision
100 days
Submission Type
Summary