K-number	K942425
Device name	PROXIDERM (TENTATIVE)
Applicant	Progressive Surgical Products, Inc.
Product code	MKY
Device class	Class I
Decision date	Nov 4, 1994
Decision	Substantially Equivalent
Regulation	878.4320

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View the full FDA submission: accessdata.fda.gov

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PROXIDERM (TENTATIVE)

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