K-number	K792458
Device name	PNEUPAC TEST SET, PT.#500-A250
Applicant	Pneupac , Ltd.
Product code	DRM
Device class	Class II
Decision date	Feb 5, 1980
Decision	Substantially Equivalent
Regulation	870.5200

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View the full FDA submission: accessdata.fda.gov

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PNEUPAC TEST SET, PT.#500-A250

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