K-number	K910661
Device name	MODEL 205 SHOCK-TRODE
Applicant	Cardiotronics, Inc.
Product code	DRO
Device class	Class II
Decision date	May 2, 1991
Decision	Substantially Equivalent
Regulation	870.5550

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View the full FDA submission: accessdata.fda.gov

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MODEL 205 SHOCK-TRODE

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