MEMOPORT C
Detector And Alarm, Arrhythmia
LITTON MEDICAL ELECTRONICS
The following data is part of a premarket notification filed by Litton Medical Electronics with the FDA for Memoport C.
Pre-market Notification Details
| Device ID | K820881 |
| 510k Number | K820881 |
| Device Name: | MEMOPORT C |
| Classification | Detector And Alarm, Arrhythmia |
| Applicant | LITTON MEDICAL ELECTRONICS 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | DSI |
| CFR Regulation Number | 870.1025 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-03-30 |
| Decision Date | 1982-05-18 |
Trademark Results [MEMOPORT C]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MEMOPORT C 73371479 not registered Dead/Abandoned |
HELLIGE, GMBH 1982-06-25 |
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