Cleared Traditional

K051595 - TSO3 OZONE STERILIZER, MODEL 125L (FDA 510(k) Clearance)

Jul 2006
Decision
405d
Days
Class 2
Risk

K051595 is an FDA 510(k) clearance for the TSO3 OZONE STERILIZER, MODEL 125L. This device is classified as a Sterilizer, Ethylene-oxide Gas (Class II - Special Controls, product code FLF).

Submitted by Tso3, Inc. (Fairport, US). The FDA issued a Cleared decision on July 26, 2006, 405 days after receiving the submission on June 16, 2005.

This device falls under the General Hospital FDA review panel. Regulated under 21 CFR 880.6860.

Submission Details

510(k) Number K051595 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 16, 2005
Decision Date July 26, 2006
Days to Decision 405 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF

Device Classification

Product Code FLF - Sterilizer, Ethylene-oxide Gas
Device Class Class II - Special Controls
CFR Regulation 21 CFR 880.6860