The following data is part of a premarket notification filed by Sigma Chemical Co. with the FDA for Dulbecco Modi Eagle Med((dme) Hybri-max (tm).
| Device ID | K870496 |
| 510k Number | K870496 |
| Device Name: | DULBECCO MODI EAGLE MED((DME) HYBRI-MAX (TM) |
| Classification | Media And Components, Synthetic Cell And Tissue Culture |
| Applicant | SIGMA CHEMICAL CO. P.O. BOX 14508 St. Louis, MO 63178 |
| Contact | David Bagley |
| Correspondent | David Bagley SIGMA CHEMICAL CO. P.O. BOX 14508 St. Louis, MO 63178 |
| Product Code | KIT |
| CFR Regulation Number | 864.2220 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-02-03 |
| Decision Date | 1987-03-30 |