The following data is part of a premarket notification filed by Sclavo, Inc. with the FDA for Cholinesterase - Acetythiocholine Substrate.
Device ID | K880199 |
510k Number | K880199 |
Device Name: | CHOLINESTERASE - ACETYTHIOCHOLINE SUBSTRATE |
Classification | Colorimetry, Cholinesterase |
Applicant | SCLAVO, INC. 5 MANSARD COURT Wayne, NJ 07470 |
Contact | King, Ph.d. |
Correspondent | King, Ph.d. SCLAVO, INC. 5 MANSARD COURT Wayne, NJ 07470 |
Product Code | DIH |
CFR Regulation Number | 862.3240 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-01-13 |
Decision Date | 1989-01-27 |