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LUTH-ALL SUB-Q NEEDLE SET

Page Type
Cleared 510(K)
510(k) Number
K042666
510(k) Type
Traditional
Applicant
Luth-All Medical Products, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2004
Days to Decision
83 days
Submission Type
Summary

LUTH-ALL SUB-Q NEEDLE SET

Page Type
Cleared 510(K)
510(k) Number
K042666
510(k) Type
Traditional
Applicant
Luth-All Medical Products, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2004
Days to Decision
83 days
Submission Type
Summary