510(k) K936181
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