K-number	K780914
Device name	PM 25 PP (BODY AID)
Applicant	Argosy Intl. (Usa), Inc.
Product code	ESD
Device class	Class I
Decision date	Jun 14, 1978
Decision	Substantially Equivalent
Regulation	874.3300

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View the full FDA submission: accessdata.fda.gov

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PM 25 PP (BODY AID)

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