The following data is part of a premarket notification filed by Ab Biodisk with the FDA for Etest Submission For Vancomycin.
Device ID | K960990 |
510k Number | K960990 |
Device Name: | ETEST SUBMISSION FOR VANCOMYCIN |
Classification | Manual Antimicrobial Susceptibility Test Systems |
Applicant | AB BIODISK DAVAGEN 10 S-171 36 Solna, SE |
Contact | Ann Bolmstrom |
Correspondent | Ann 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 |