K-number	K921326
Device name	DADE RECOMBOPLASTIN S
Applicant	Baxter Diagnostics, Inc.
Product code	GJS
Device class	Class II
Decision date	Jul 27, 1992
Decision	Substantially Equivalent
Regulation	864.7750

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View the full FDA submission: accessdata.fda.gov

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DADE RECOMBOPLASTIN S

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