The following data is part of a premarket notification filed by Dade Behring, Inc. with the FDA for Microstrep Plus Panel With Ampicillin.
| Device ID | K021037 |
| 510k Number | K021037 |
| Device Name: | MICROSTREP PLUS PANEL WITH AMPICILLIN |
| Classification | Manual Antimicrobial Susceptibility Test Systems |
| Applicant | DADE BEHRING, INC. 2040 ENTERPRISE BLVD. West Sacramento, CA 95691 |
| Contact | Cynthia Van Duker |
| Correspondent | Cynthia Van Duker DADE BEHRING, INC. 2040 ENTERPRISE BLVD. West Sacramento, CA 95691 |
| Product Code | JWY |
| CFR Regulation Number | 866.1640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-04-01 |
| Decision Date | 2002-05-06 |
| Summary: | summary |