The following data is part of a premarket notification filed by Analytical Products, Inc. with the FDA for Api 20e/uniscept 20e.
Device ID | K924814 |
510k Number | K924814 |
Device Name: | API 20E/UNISCEPT 20E |
Classification | Kit, Identification, Enterobacteriaceae |
Applicant | ANALYTICAL PRODUCTS, INC. 200 EXPRESS STREET Plainview , NY 11803 - |
Contact | Valerie L Vargo |
Correspondent | Valerie L Vargo ANALYTICAL PRODUCTS, INC. 200 EXPRESS STREET Plainview , NY 11803 - |
Product Code | JSS |
CFR Regulation Number | 866.2660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-09-25 |
Decision Date | 1993-03-11 |