K-number	K860770
Device name	AM-100 I/A AMPAC
Applicant	Dravon Medical, Inc.
Product code	HQC
Device class	Class II
Decision date	Apr 21, 1986
Decision	Substantially Equivalent
Regulation	886.4670

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View the full FDA submission: accessdata.fda.gov

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AM-100 I/A AMPAC

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