FDA 510(k) Applications Submitted by KERRY A KAHN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K993777 | 11/08/1999 | DISPOSABLE AND REUSABLE BALL AND LOOP ELECTRODES | R-GROUP INTL. |
| K001233 | 04/17/2000 | ACTI-FLEX FLUID DELIVERY SYSTEM OR ACTI-FLEX F D S | R-GROUP INTL. |
| K001599 | 05/24/2000 | ACTI-FLEX IV ADMINISTRATION SET | R-GROUP INTL. |
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