The following data is part of a premarket notification filed by Advanced Instrumentations, Inc. with the FDA for Ecg Series Electrocardiograph.
| Device ID | K111805 |
| 510k Number | K111805 |
| Device Name: | ECG SERIES ELECTROCARDIOGRAPH |
| Classification | Electrocardiograph |
| Applicant | ADVANCED INSTRUMENTATIONS, INC. 601 W 20 ST Hialeah, FL 33010 |
| Contact | Jorge Millan |
| Correspondent | Jorge Millan ADVANCED INSTRUMENTATIONS, INC. 601 W 20 ST Hialeah, FL 33010 |
| Product Code | DPS |
| CFR Regulation Number | 870.2340 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-06-27 |
| Decision Date | 2011-08-24 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| B510ECG3PLUS1 | K111805 | 000 |
| B510ECG12C1 | K111805 | 000 |
| B510ECG3F1 | K111805 | 000 |
| B510ECG121 | K111805 | 000 |