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GRIPPER PLUS NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K021999
510(k) Type
Traditional
Applicant
DELTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/2002
Days to Decision
55 days
Submission Type
Summary

GRIPPER PLUS NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K021999
510(k) Type
Traditional
Applicant
DELTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/2002
Days to Decision
55 days
Submission Type
Summary