The following data is part of a premarket notification filed by American Optical Corp. with the FDA for Aod4000 Disposable Pak.
Device ID | K931357 |
510k Number | K931357 |
Device Name: | AOD4000 DISPOSABLE PAK |
Classification | Unit, Phacofragmentation |
Applicant | AMERICAN OPTICAL CORP. 19 HAMMOND SUITE 505 Irvine, CA 92718 |
Contact | Herbert Cameron |
Correspondent | Herbert Cameron AMERICAN OPTICAL CORP. 19 HAMMOND SUITE 505 Irvine, CA 92718 |
Product Code | HQC |
CFR Regulation Number | 886.4670 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-03-17 |
Decision Date | 1994-01-25 |