510(k) K212174

STERRAD 100NX Sterilizer with ALLClear Technology by Advanced Sterilization Products, Inc. — Product Code MLR

K212174 is an FDA 510(k) premarket notification submitted by Advanced Sterilization Products, Inc. for the device "STERRAD 100NX Sterilizer with ALLClear Technology". The FDA issued a decision of Substantially Equivalent on October 9, 2021. The device falls under product code MLR (Sterilizer, Chemical), a Class II device regulated under 21 CFR 880.6860. Advanced Sterilization Products, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 9, 2021
Date Received
July 12, 2021
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Sterilizer, Chemical
Device Class
Class II
Regulation Number
880.6860
Review Panel
HO
Submission Type