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SHELLY PROTECTED AV FISTULA NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K993187
510(k) Type
Traditional
Applicant
DIASOL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1999
Days to Decision
43 days
Submission Type
Statement

SHELLY PROTECTED AV FISTULA NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K993187
510(k) Type
Traditional
Applicant
DIASOL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1999
Days to Decision
43 days
Submission Type
Statement