K-number	K915636
Device name	GLOVE CHECK PATIENT EXAMINATION GLOVE LEAK DETECT.
Applicant	Associated Ent., Inc.
Product code	LDQ
Device class	Class unclassified
Decision date	Jul 13, 1992
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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GLOVE CHECK PATIENT EXAMINATION GLOVE LEAK DETECT.

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