Last synced on 25 November 2022 at 11:04 pm

FUTREX-6100/XL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963271
510(k) Type
Traditional
Applicant
FUTREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/1998
Days to Decision
729 days
Submission Type
Statement

FUTREX-6100/XL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963271
510(k) Type
Traditional
Applicant
FUTREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/19/1998
Days to Decision
729 days
Submission Type
Statement