K-number	K904021
Device name	PNEUMOTHORAX KIT, MODIFICATION
Applicant	Arrow Intl., Inc.
Product code	JDC
Device class	Class II
Decision date	Oct 9, 1990
Decision	Substantially Equivalent
Regulation	888.3150

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View the full FDA submission: accessdata.fda.gov

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PNEUMOTHORAX KIT, MODIFICATION

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