Last synced on 30 May 2025 at 11:05 pm

AKROTECH 4000T KINETIC TURNING LOW AIR LOSS SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962123
510(k) Type
Traditional
Applicant
LUMEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/1996
Days to Decision
48 days
Submission Type
Summary

AKROTECH 4000T KINETIC TURNING LOW AIR LOSS SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962123
510(k) Type
Traditional
Applicant
LUMEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/1996
Days to Decision
48 days
Submission Type
Summary