K-number	K922942
Device name	PRO-SCOPE MODEL # PS-4000
Applicant	Pro-Den Systems, Inc.
Product code	EIA
Device class	Class I
Decision date	Sep 10, 1993
Decision	Substantially Equivalent
Regulation	872.6640

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View the full FDA submission: accessdata.fda.gov

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PRO-SCOPE MODEL # PS-4000

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