The following data is part of a premarket notification filed by Eyecotech Corp. with the FDA for Eyecotech Corp.
| Device ID | K941414 |
| 510k Number | K941414 |
| Device Name: | EYECOTECH CORP |
| Classification | Frame, Spectacle |
| Applicant | EYECOTECH CORP. 2729 S. PEPPERDALE DR. Rowland Hts., CA 91748 |
| Contact | Jennifer Kuo |
| Correspondent | Jennifer Kuo EYECOTECH CORP. 2729 S. PEPPERDALE DR. Rowland Hts., CA 91748 |
| Product Code | HQZ |
| CFR Regulation Number | 886.5842 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-03-23 |
| Decision Date | 1994-07-12 |