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AXON SYSTEMS SUBDERMAL NEEDLE ELECTRODES

Page Type
Cleared 510(K)
510(k) Number
K050194
510(k) Type
Traditional
Applicant
AXON SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/2005
Days to Decision
89 days
Submission Type
Summary

AXON SYSTEMS SUBDERMAL NEEDLE ELECTRODES

Page Type
Cleared 510(K)
510(k) Number
K050194
510(k) Type
Traditional
Applicant
AXON SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/2005
Days to Decision
89 days
Submission Type
Summary