The following data is part of a premarket notification filed by Dade Microscan, Inc. with the FDA for Microscan Synergies Plus.
Device ID | K023202 |
510k Number | K023202 |
Device Name: | MICROSCAN SYNERGIES PLUS |
Classification | Manual Antimicrobial Susceptibility Test Systems |
Applicant | DADE MICROSCAN, INC. 1584 ENTERPRISE BLVD. West Sacramento, CA 95691 |
Contact | Cynthia Van Duker |
Correspondent | Cynthia Van Duker DADE MICROSCAN, INC. 1584 ENTERPRISE BLVD. West Sacramento, CA 95691 |
Product Code | JWY |
CFR Regulation Number | 866.1640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-09-25 |
Decision Date | 2002-10-23 |