K-number	K902850
Device name	ZEPPELIN INSTRUMENTS
Applicant	Ruggles Corp.
Product code	HAO
Device class	Class I
Decision date	Jul 18, 1990
Decision	Substantially Equivalent
Regulation	882.4535

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View the full FDA submission: accessdata.fda.gov

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ZEPPELIN INSTRUMENTS

Everything you need for a 510(k) submission. Nothing you don't.