Last synced on 2 May 2025 at 11:05 pm

LUMEX WHEELCHAIRS (SER. 1000, 3000, 4000, 5000, TILT-IN-SPACE, 6000, MRI)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K944574
510(k) Type
Traditional
Applicant
LUMEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/1994
Days to Decision
28 days
Submission Type
Summary

LUMEX WHEELCHAIRS (SER. 1000, 3000, 4000, 5000, TILT-IN-SPACE, 6000, MRI)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K944574
510(k) Type
Traditional
Applicant
LUMEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/1994
Days to Decision
28 days
Submission Type
Summary