FDA 510(k) Applications Submitted by STEPHAN KRIETEMEYER
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K032004 | 06/30/2003 | AQUABOSS ECORO DIA 50 | LAUER LTD., HONG KONG |
| K124059 | 12/31/2012 | AQUABOSS ECORO DIA I (HT); AQUABOSS ECORO DIA II (HT) | LAUER MEMBRAN WASSERTECHNIK GMBH |
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