FDA 510(k) Applications Submitted by OLDELFT CORP. OF AMERICA
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K980296 | 01/27/1998 | OLDELFT DIGIDELCA | OLDELFT CORP. OF AMERICA |
| K973219 | 08/27/1997 | AMBER DU | OLDELFT CORP. OF AMERICA |
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