The following data is part of a premarket notification filed by Lic-orthion with the FDA for Citomat Autoclaves.
Device ID | K843234 |
510k Number | K843234 |
Device Name: | CITOMAT AUTOCLAVES |
Classification | Sterilizer, Boiling Water |
Applicant | LIC-ORTHION 2101 L ST. NW Washington , DC 20037 - |
Contact | Rodney R Munsey |
Correspondent | Rodney R Munsey LIC-ORTHION 2101 L ST. NW Washington , DC 20037 - |
Product Code | ECG |
CFR Regulation Number | 872.6710 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-08-17 |
Decision Date | 1984-10-25 |