The following data is part of a premarket notification filed by Abtox, Inc. with the FDA for Abtox Plazlyte Process Monitor.
Device ID | K923442 |
510k Number | K923442 |
Device Name: | ABTOX PLAZLYTE PROCESS MONITOR |
Classification | Sterilizer, Ethylene-oxide Gas |
Applicant | ABTOX, INC. 104 TERRACE DR. Mundelein, IL 60060 |
Contact | Ross A Caputo |
Correspondent | Ross A Caputo ABTOX, INC. 104 TERRACE DR. Mundelein, IL 60060 |
Product Code | FLF |
CFR Regulation Number | 880.6860 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-07-13 |
Decision Date | 1994-12-22 |