K-number	K923028
Device name	TURKEL PNEUMOTHORAX KIT
Applicant	Symbiosis Corp.
Product code	GCB
Device class	Class I
Decision date	Aug 4, 1992
Decision	Substantially Equivalent
Regulation	878.4200

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View the full FDA submission: accessdata.fda.gov

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TURKEL PNEUMOTHORAX KIT

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