K-number	K802025
Device name	BALLOON RETENTION CHEST CATHETER
Applicant	Loseff Medical Designers, Ltd.
Product code	GBA
Device class	Class I
Decision date	Sep 26, 1980
Decision	Substantially Equivalent
Regulation	878.4200

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View the full FDA submission: accessdata.fda.gov

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BALLOON RETENTION CHEST CATHETER

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