Last synced on 25 April 2025 at 11:05 pm

LifeOutcomes C-Quest™ Blood Culture Sampling Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231282
510(k) Type
Traditional
Applicant
LifeOutcomes LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/2024
Days to Decision
268 days
Submission Type
Summary

LifeOutcomes C-Quest™ Blood Culture Sampling Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231282
510(k) Type
Traditional
Applicant
LifeOutcomes LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/2024
Days to Decision
268 days
Submission Type
Summary