The following data is part of a premarket notification filed by Brentwood Medical Technology Corp. with the FDA for Midmark Iqecg.
| Device ID | K103640 |
| 510k Number | K103640 |
| Device Name: | MIDMARK IQECG |
| Classification | Electrocardiograph |
| Applicant | BRENTWOOD MEDICAL TECHNOLOGY CORP. 3722 AVE. SAUSALITO Irvine, CA 92606 |
| Contact | Greg Holland |
| Correspondent | Greg Holland BRENTWOOD MEDICAL TECHNOLOGY CORP. 3722 AVE. SAUSALITO Irvine, CA 92606 |
| Product Code | DPS |
| CFR Regulation Number | 870.2340 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-12-13 |
| Decision Date | 2011-03-22 |
| Summary: | summary |