Last synced on 4 February 2023 at 10:33 pm

REXTON'S HORIZION FAMILY OF MULTIPLE SITUATION, SINGLE CHANNEL PROGRAMMBALE INSTRUMENTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K954922
510(k) Type
Traditional
Applicant
REXTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/1996
Days to Decision
83 days
Submission Type
Summary