K-number	K821308
Device name	ESPREE' GUEDEL ESPREE BERMAN AIRWAY
Applicant	Esp Plastics, Inc.
Product code	CAE
Device class	Class I
Decision date	May 21, 1982
Decision	Substantially Equivalent
Regulation	868.5110

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View the full FDA submission: accessdata.fda.gov

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ESPREE' GUEDEL ESPREE BERMAN AIRWAY

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