RABEA DEVICE, MODEL PXXXXXX (K990345) — FDA 510(k) Clearance | Predicase

K-number	K990345
Device name	RABEA DEVICE, MODEL PXXXXXX
Applicant	Signus Medizintechnik GmbH
Product code	JDK
Device class	Class II
Decision date	Jul 30, 1999
Decision	Unknown
Regulation	878.3300

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Source

View the full FDA submission: accessdata.fda.gov

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