Cleared Traditional

K951703 - TAMPER EVIDENT ARROWS WITH AND WITHOUT ...

K951703 is an FDA 510(k) clearance for TAMPER EVIDENT ARROWS WITH AND WITHOUT ..., manufactured by Products For Medicine. The device is a Class 2 General Hospital device with product code LRT cleared through the Traditional 510(k) pathway after a 77-day FDA review.

K951703 · Products For Medicine · General Hospital
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Jun 1995
Decision
77d
Days
Class 2
Risk

K951703 is an FDA 510(k) clearance for the TAMPER EVIDENT ARROWS WITH AND WITHOUT STERILIZATION INDICATORS. Classified as Indicator, Sterilization (product code LRT), Class II - Special Controls.

Submitted by Products For Medicine (Irvine, US). The FDA issued a Cleared decision on June 28, 1995 after a review of 77 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.

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FDA 510(k) Submission Details - K951703

510(k) Number K951703 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 12, 1995
Decision Date June 28, 1995
Days to Decision 77 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
52d faster than avg
Panel avg: 129d · This submission: 77d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LRT Device Classification - Class 2, Special Controls

Product Code LRT Indicator, Sterilization
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.