The following data is part of a premarket notification filed by Blublocker Corp. with the FDA for Blublocker Sunglasses.
| Device ID | K900382 |
| 510k Number | K900382 |
| Device Name: | BLUBLOCKER SUNGLASSES |
| Classification | Sunglasses (non-prescription Including Photosensitive) |
| Applicant | BLUBLOCKER CORP. 3100 DUNDEE RD SUITE 802 Northbrook, IL 60062 |
| Contact | Joseph Sugarman |
| Correspondent | Joseph Sugarman BLUBLOCKER CORP. 3100 DUNDEE RD SUITE 802 Northbrook, IL 60062 |
| Product Code | HQY |
| CFR Regulation Number | 886.5850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-01-25 |
| Decision Date | 1990-02-13 |