The following data is part of a premarket notification filed by Intel Corp. with the FDA for Intel Health Guide, Model: Phs6000.
Device ID | K080798 |
510k Number | K080798 |
Device Name: | INTEL HEALTH GUIDE, MODEL: PHS6000 |
Classification | Transmitters And Receivers, Physiological Signal, Radiofrequency |
Applicant | INTEL CORP. 1900 PRAIRIE CITY RD., FM7-197 Folsom, CA 95630 |
Contact | Tae-woong Koo |
Correspondent | Tae-woong Koo INTEL CORP. 1900 PRAIRIE CITY RD., FM7-197 Folsom, CA 95630 |
Product Code | DRG |
CFR Regulation Number | 870.2910 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-03-20 |
Decision Date | 2008-06-27 |
Summary: | summary |