The following data is part of a premarket notification filed by Lakewood Biochemical Co., Inc. with the FDA for P4802 Bea.
| Device ID | K870339 |
| 510k Number | K870339 |
| Device Name: | P4802 BEA |
| Classification | Culture Media, Selective And Differential |
| Applicant | LAKEWOOD BIOCHEMICAL CO., INC. 2111 IRVING BLVD. Dallas, TX 75207 |
| Contact | John E Pedigo |
| Correspondent | John E Pedigo LAKEWOOD BIOCHEMICAL CO., INC. 2111 IRVING BLVD. Dallas, TX 75207 |
| Product Code | JSI |
| CFR Regulation Number | 866.2360 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-01-28 |
| Decision Date | 1987-02-13 |