Last synced on 26 May 2023 at 11:04 pm

SHELLY PROTECTED AV FISTULA NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992653
510(k) Type
Traditional
Applicant
DIASOL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/1999
Days to Decision
82 days
Submission Type
Statement

SHELLY PROTECTED AV FISTULA NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992653
510(k) Type
Traditional
Applicant
DIASOL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/1999
Days to Decision
82 days
Submission Type
Statement