K-number	K963304
Device name	STRYKER TEMPEST ORTHOPEDIC PUMP
Applicant	Stryker Endoscopy
Product code	HRX
Device class	Class II
Decision date	Jan 22, 1997
Decision	Substantially Equivalent
Regulation	888.1100

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View the full FDA submission: accessdata.fda.gov

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STRYKER TEMPEST ORTHOPEDIC PUMP

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