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RK EPIDURAL NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K072005
510(k) Type
Traditional
Applicant
EPIMED INTERNATIONAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/2008
Days to Decision
199 days
Submission Type
Summary

RK EPIDURAL NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K072005
510(k) Type
Traditional
Applicant
EPIMED INTERNATIONAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/2008
Days to Decision
199 days
Submission Type
Summary