The following data is part of a premarket notification filed by Ab Biodisk with the FDA for Etest Submission For Imipenem.
| Device ID | K960989 |
| 510k Number | K960989 |
| Device Name: | ETEST SUBMISSION FOR IMIPENEM |
| Classification | Manual Antimicrobial Susceptibility Test Systems |
| Applicant | AB BIODISK DAVAGEN 10 S-171 36 Solna, SE |
| Contact | Anne Bolmstrom |
| Correspondent | Anne Bolmstrom AB BIODISK DAVAGEN 10 S-171 36 Solna, SE |
| Product Code | JWY |
| CFR Regulation Number | 866.1640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-03-11 |
| Decision Date | 1996-05-20 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 03573026377953 | K960989 | 000 |
| 03573026252953 | K960989 | 000 |
| 03573026618216 | K960989 | 000 |