FDA 510(k) Applications Submitted by KLAUS RUDOLF
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K000638 | 02/25/2000 | RESPONDER 3000 | GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES GMBH |
| K950989 | 03/03/1995 | CARDIOSMART | HELLIGE GMBH |
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