The following data is part of a premarket notification filed by Zest Anchors, Inc. with the FDA for Zest Anchor Advanced Generation.
Device ID | K925700 |
510k Number | K925700 |
Device Name: | ZEST ANCHOR ADVANCED GENERATION |
Classification | Attachment, Precision, All |
Applicant | ZEST ANCHORS, INC. 2061 WINERIDGE PL., SUITE 100 Escondido, CA 92029 |
Contact | Paul Zest |
Correspondent | Paul Zest ZEST ANCHORS, INC. 2061 WINERIDGE PL., SUITE 100 Escondido, CA 92029 |
Product Code | EGG |
CFR Regulation Number | 872.3165 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-11-12 |
Decision Date | 1994-04-07 |