The following data is part of a premarket notification filed by Midmark Corp. with the FDA for Midmark M-11 Ultraclave Steam Sterilizer.
Device ID | K936181 |
510k Number | K936181 |
Device Name: | MIDMARK M-11 ULTRACLAVE STEAM STERILIZER |
Classification | Sterilizer, Steam |
Applicant | MIDMARK CORP. 60 VISTA DR. P.O. BOX 286 Versailles, OH 45380 |
Contact | Bradley K Seiden |
Correspondent | Bradley K Seiden MIDMARK CORP. 60 VISTA DR. P.O. BOX 286 Versailles, OH 45380 |
Product Code | FLE |
CFR Regulation Number | 880.6880 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-12-27 |
Decision Date | 1994-11-30 |