Last synced on 14 November 2025 at 11:06 pm

LINEAR LIFT DEVICE

Page Type
Cleared 510(K)
510(k) Number
K881676
510(k) Type
Traditional
Applicant
CYBEX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/25/1990
Days to Decision
736 days

LINEAR LIFT DEVICE

Page Type
Cleared 510(K)
510(k) Number
K881676
510(k) Type
Traditional
Applicant
CYBEX
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/25/1990
Days to Decision
736 days