FDA 510(k) Applications Submitted by KRISTI KUNKEL
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K960819 | 02/29/1996 | HELIODENT DS | PELTON & CRANE CO. |
| K962071 | 05/28/1996 | SPIRIT S1/S2 | PELTON & CRANE CO. |
| K945117 | 10/18/1994 | DELTA | PELTON & CRANE CO. |
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