K-number	K955439
Device name	THE REEL THING (MODIFICATION)
Applicant	Biomedical Devices, Inc.
Product code	GBX
Device class	Class I
Decision date	Dec 26, 1995
Decision	Substantially Equivalent
Regulation	878.4200

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View the full FDA submission: accessdata.fda.gov

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THE REEL THING (MODIFICATION)

Everything you need for a 510(k) submission. Nothing you don't.