FDA 510(k) Applications Submitted by MEMTEC CORP.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K102723 | 09/21/2010 | MODEL 950-12L HOLTER RECORDER WITHOUT ANALYSIS | MEMTEC CORP. |
| K103427 | 11/22/2010 | MOBILEECG SYSTEM | MEMTEC CORP. |
| K944180 | 08/26/1994 | MODEL 700 | MEMTEC CORP. |
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