K-number	K930840
Device name	POST-MYDS(TM)
Applicant	Aukland Medical Plastics, Inc.
Product code	HOY
Device class	Class I
Decision date	Mar 1, 1994
Decision	Substantially Equivalent
Regulation	886.4750

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View the full FDA submission: accessdata.fda.gov

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POST-MYDS(TM)

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