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SHELLY PROTECTED AV FISTULA NEEDLE

Page Type
Cleared 510(K)
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)
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