The following data is part of a premarket notification filed by Vital Connect, Inc with the FDA for Vitalconnect Platform By Vital Connect Inc..
| Device ID | K132447 |
| 510k Number | K132447 |
| Device Name: | VITALCONNECT PLATFORM BY VITAL CONNECT INC. |
| Classification | Transmitters And Receivers, Physiological Signal, Radiofrequency |
| Applicant | Vital Connect, Inc 900 E. Hamilton Ave. Ste # 500 Campbell, CA 95008 |
| Contact | Sam Mostafavi |
| Correspondent | Sam Mostafavi Vital Connect, Inc 900 E. Hamilton Ave. Ste # 500 Campbell, CA 95008 |
| Product Code | DRG |
| CFR Regulation Number | 870.2910 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-08-06 |
| Decision Date | 2014-04-03 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00850490007047 | K132447 | 000 |
| 00850490007016 | K132447 | 000 |
| 00850490007023 | K132447 | 000 |