Last synced on 23 September 2022 at 11:05 pm

PNEUMO-WEDGE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921143
510(k) Type
Traditional
Applicant
KANSAS CREATIVE DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/1992
Days to Decision
184 days
Submission Type
Summary

PNEUMO-WEDGE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921143
510(k) Type
Traditional
Applicant
KANSAS CREATIVE DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/1992
Days to Decision
184 days
Submission Type
Summary