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BABYLANCE HEEL INCISION DEVICE , MODELS BLP50, BLP200, BLN50, BLN200

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101417
510(k) Type
Abbreviated
Applicant
MEDIPURPOSE PTE. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/2010
Days to Decision
152 days
Submission Type
Summary

BABYLANCE HEEL INCISION DEVICE , MODELS BLP50, BLP200, BLN50, BLN200

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101417
510(k) Type
Abbreviated
Applicant
MEDIPURPOSE PTE. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/2010
Days to Decision
152 days
Submission Type
Summary