K-number	K013719
Device name	BECKER BAND CRANIAL REMOLDING ORTHOSIS
Applicant	Becker Orthopedic Appliance Co.
Product code	MVA
Device class	Class II
Decision date	Feb 5, 2002
Decision	Substantially Equivalent
Regulation	882.5970

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View the full FDA submission: accessdata.fda.gov

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BECKER BAND CRANIAL REMOLDING ORTHOSIS

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