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BABYLANCE HEEL INCISION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K130132
510(k) Type
Special
Applicant
MEDIPURPOSE PTE. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/2013
Days to Decision
24 days
Submission Type
Summary

BABYLANCE HEEL INCISION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K130132
510(k) Type
Special
Applicant
MEDIPURPOSE PTE. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/2013
Days to Decision
24 days
Submission Type
Summary