The following data is part of a premarket notification filed by Pasco Laboratories, Inc. with the FDA for Modification To Pasco Mic And Mic/id Panels.
Device ID | K001887 |
510k Number | K001887 |
Device Name: | MODIFICATION TO PASCO MIC AND MIC/ID PANELS |
Classification | Manual Antimicrobial Susceptibility Test Systems |
Applicant | PASCO LABORATORIES, INC. 12750 WEST 42ND AVE. Wheat Ridge, CO 80033 |
Contact | Linda K Dillion |
Correspondent | Linda K Dillion PASCO LABORATORIES, INC. 12750 WEST 42ND AVE. Wheat Ridge, CO 80033 |
Product Code | JWY |
CFR Regulation Number | 866.1640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-06-21 |
Decision Date | 2000-08-09 |