Cleared Traditional

K051157 - INSTRU-SAFE INSTRUMENT PROTECTION SYSTEMS (FDA 510(k) Clearance)

Sep 2005
Decision
119d
Days
Class 2
Risk

K051157 is an FDA 510(k) clearance for the INSTRU-SAFE INSTRUMENT PROTECTION SYSTEMS. This device is classified as a Sterilization Wrap Containers, Trays, Cassettes & Other Accessories (Class II - Special Controls, product code KCT).

Submitted by Micromedics, Inc. (St. Paul, US). The FDA issued a Cleared decision on September 1, 2005, 119 days after receiving the submission on May 5, 2005.

This device falls under the General Hospital FDA review panel. Regulated under 21 CFR 880.6850.

Submission Details

510(k) Number K051157 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 05, 2005
Decision Date September 01, 2005
Days to Decision 119 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement

Device Classification

Product Code KCT — Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
Device Class Class II - Special Controls
CFR Regulation 21 CFR 880.6850

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