Last synced on 14 November 2025 at 11:06 pm

Spacelabs Lifescreen PRO Analyzer

Page Type
Cleared 510(K)
510(k) Number
K201921
510(k) Type
Traditional
Applicant
Spacelabs Healthcare Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
3/26/2021
Days to Decision
259 days
Submission Type
Summary

Spacelabs Lifescreen PRO Analyzer

Page Type
Cleared 510(K)
510(k) Number
K201921
510(k) Type
Traditional
Applicant
Spacelabs Healthcare Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
3/26/2021
Days to Decision
259 days
Submission Type
Summary