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SITERITE NEEDLE GUIDE

Page Type
Cleared 510(K)
510(k) Number
K903158
510(k) Type
Traditional
Applicant
DYMAX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/1990
Days to Decision
71 days

SITERITE NEEDLE GUIDE

Page Type
Cleared 510(K)
510(k) Number
K903158
510(k) Type
Traditional
Applicant
DYMAX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/1990
Days to Decision
71 days