BIOFIND
Device, Galvanic Skin Response Measurement
BIO-SCAN, INC.
The following data is part of a premarket notification filed by Bio-scan, Inc. with the FDA for Biofind.
Pre-market Notification Details
| Device ID | K003480 |
| 510k Number | K003480 |
| Device Name: | BIOFIND |
| Classification | Device, Galvanic Skin Response Measurement |
| Applicant | BIO-SCAN, INC. 6 WALDEN RD. Corrales, NM 87048 |
| Contact | Butch Smith |
| Correspondent | Butch Smith BIO-SCAN, INC. 6 WALDEN RD. Corrales, NM 87048 |
| Product Code | GZO |
| CFR Regulation Number | 882.1540 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-11-09 |
| Decision Date | 2001-05-11 |
Trademark Results [BIOFIND]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 BIOFIND 76029908 2670887 Dead/Cancelled |
KMP ASSOCIATES LIMITED 2000-04-20 |
 BIOFIND 75085162 2143937 Dead/Cancelled |
BioScan, Inc. 1996-04-08 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.