K-number	K091462
Device name	SPECTRA MEDICAL SAFETY SCAPEL
Applicant	Spectra, Inc.
Product code	GDZ
Device class	Class I
Decision date	Dec 15, 2009
Decision	Substantially Equivalent
Regulation	878.4800

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View the full FDA submission: accessdata.fda.gov

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SPECTRA MEDICAL SAFETY SCAPEL

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