Cleared Traditional

K951601 - MED-TEC STRING RETICLE TRAY

K951601 is the FDA 510(k) clearance for MED-TEC STRING RETICLE TRAY by Medtec, Inc.. It is a Class 1 Radiology device (product code IWE) cleared through the Traditional 510(k) pathway after a 34-day FDA review.

K951601 · Medtec, Inc. · Radiology device
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May 1995
Decision
34d
Days
Class 1
Risk

K951601 is an FDA 510(k) clearance for the MED-TEC STRING RETICLE TRAY. Classified as Monitor, Patient Position, Light-beam (product code IWE), Class I - General Controls.

Submitted by Medtec, Inc. (Orange City, US). The FDA issued a Cleared decision on May 11, 1995 after a review of 34 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.5780 - the FDA radiology and imaging software oversight 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 Medtec, Inc. devices

Submission Details

510(k) Number K951601 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 07, 1995
Decision Date May 11, 1995
Days to Decision 34 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
73d faster than avg
Panel avg: 107d · This submission: 34d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code IWE Monitor, Patient Position, Light-beam
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 892.5780
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - IWE Monitor, Patient Position, Light-beam

All 7
Devices cleared under the same product code (IWE) and FDA review panel - the closest regulatory comparables to K951601.
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LASER ALIGNMENT TOOL
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K941169 · Medtec, Inc. · Jul 1994
TEC 2100 (MODEL MT-LPLGD)
K935760 · Medtec, Inc. · Jan 1994