K-number	K781245
Device name	LUNG EXER. BAG, POST-OP, MODIFIED
Applicant	Dytek Corp.
Product code	BWF
Device class	Class II
Decision date	Sep 20, 1978
Decision	Substantially Equivalent
Regulation	868.5690

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View the full FDA submission: accessdata.fda.gov

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LUNG EXER. BAG, POST-OP, MODIFIED

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