FDA 510(k) Applications Submitted by KOHLER MEDIZINTECHNIK GMBH & CO. KG
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K980616 | 02/18/1998 | PERMAFIX CHAIRSIDE SOFT DENTURE RELINING (7010) (7011-13) (7014-15) | KOHLER MEDIZINTECHNIK GMBH & CO. KG |
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