510(k) K936181

MIDMARK M-11 ULTRACLAVE STEAM STERILIZER by Midmark Corp. — Product Code FLE

K936181 is an FDA 510(k) premarket notification submitted by Midmark Corp. for the device "MIDMARK M-11 ULTRACLAVE STEAM STERILIZER". The FDA issued a decision of Substantially Equivalent on November 30, 1994. The device falls under product code FLE (Sterilizer, Steam), a Class II device regulated under 21 CFR 880.6880. Midmark Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 30, 1994
Date Received
December 27, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Sterilizer, Steam
Device Class
Class II
Regulation Number
880.6880
Review Panel
HO
Submission Type