K-number	K864190
Device name	E-Z HOLD - #4060
Applicant	John F. Greer Co., Inc.
Product code	KMK
Device class	Class I
Decision date	Jan 14, 1987
Decision	Substantially Equivalent
Regulation	880.5210

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View the full FDA submission: accessdata.fda.gov

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E-Z HOLD - #4060

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