The following data is part of a premarket notification filed by Hass Corp. with the FDA for Hass Zirtooth Model Zortooth H. Zirtooth T. Zirtoothc, Zirtooth P.
| Device ID | K102305 |
| 510k Number | K102305 |
| Device Name: | HASS ZIRTOOTH MODEL ZORTOOTH H. ZIRTOOTH T. ZIRTOOTHC, ZIRTOOTH P |
| Classification | Powder, Porcelain |
| Applicant | HASS CORP. 2341 W. CRESCENT AVE. #3 Anaheim, CA 92801 |
| Contact | Priscilla Chung |
| Correspondent | Priscilla Chung HASS CORP. 2341 W. CRESCENT AVE. #3 Anaheim, CA 92801 |
| Product Code | EIH |
| CFR Regulation Number | 872.6660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-08-16 |
| Decision Date | 2010-12-03 |
| Summary: | summary |