Last synced on 25 July 2025 at 11:06 pm

LiftUp (Ref. Nr.: 200.56.01), LiftUp Kit (Ref. Nr.: 200.56.02)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221385
510(k) Type
Traditional
Applicant
Ovesco Endoscopy AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
8/11/2022
Days to Decision
90 days
Submission Type
Statement

LiftUp (Ref. Nr.: 200.56.01), LiftUp Kit (Ref. Nr.: 200.56.02)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221385
510(k) Type
Traditional
Applicant
Ovesco Endoscopy AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
8/11/2022
Days to Decision
90 days
Submission Type
Statement