Last synced on 25 April 2025 at 11:05 pm

EXEL AVF SINGLE NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963658
510(k) Type
Traditional
Applicant
EXEL INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/1998
Days to Decision
609 days
Submission Type
Statement

EXEL AVF SINGLE NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963658
510(k) Type
Traditional
Applicant
EXEL INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/1998
Days to Decision
609 days
Submission Type
Statement