K-number	K854697
Device name	TUBING HANDPIECE REPLACEMENT
Applicant	Almore Intl., Inc.
Product code	EFB
Device class	Class I
Decision date	Mar 6, 1986
Decision	Substantially Equivalent
Regulation	872.4200

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View the full FDA submission: accessdata.fda.gov

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TUBING HANDPIECE REPLACEMENT

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