Cleared Traditional

K110369 - INDISTRIP GREEN

K110369 is an FDA 510(k) clearance for INDISTRIP GREEN, manufactured by Indilab, Inc.. The device is a Class 2 General Hospital device with product code JOJ cleared through the Traditional 510(k) pathway after a 87-day FDA review.

K110369 · Indilab, Inc. · General Hospital
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May 2011
Decision
87d
Days
Class 2
Risk

K110369 is an FDA 510(k) clearance for the INDISTRIP GREEN. Classified as Indicator, Physical/chemical Sterilization Process (product code JOJ), Class II - Special Controls.

Submitted by Indilab, Inc. (Chicago, US). The FDA issued a Cleared decision on May 6, 2011 after a review of 87 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.2800 - the FDA general hospital device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Indilab, Inc. devices

FDA 510(k) Submission Details - K110369

510(k) Number K110369 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 08, 2011
Decision Date May 06, 2011
Days to Decision 87 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
42d faster than avg
Panel avg: 129d · This submission: 87d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JOJ Device Classification - Class 2, Special Controls

Product Code JOJ Indicator, Physical/chemical Sterilization Process
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.2800
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General Hospital devices follow this clearance model.

Regulatory Peers - JOJ Indicator, Physical/chemical Sterilization Process

All 223
Devices cleared under the same product code (JOJ) and FDA review panel - the closest regulatory comparables to K110369.
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K110253 · Dana Products, Inc. · Apr 2011
SPSMEDICAL VAPORIZED HYDROGEN PEROXIDE CHEMICAL INDICATORS
K110152 · Spsmedical Supply Corp. · Apr 2011
STERRAD CHEMICAL INDICATOR STRIP
K103218 · Advanced Sterilization Products · Apr 2011