Last synced on 14 November 2025 at 11:06 pm

SITERITE NEEDLE GUIDE (MODIFIED)

Page Type
Cleared 510(K)
510(k) Number
K931403
510(k) Type
Traditional
Applicant
DYMAX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/1993
Days to Decision
130 days
Submission Type
Summary

SITERITE NEEDLE GUIDE (MODIFIED)

Page Type
Cleared 510(K)
510(k) Number
K931403
510(k) Type
Traditional
Applicant
DYMAX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/1993
Days to Decision
130 days
Submission Type
Summary