Cleared Traditional

K830706 - E.T. STRAP #6000 (FDA 510(k) Clearance)

Class I Anesthesiology device.

K830706 · Rnd Medical Products, Inc. · Anesthesiology device
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Apr 1983
Decision
52d
Days
Class 1
Risk

K830706 is an FDA 510(k) clearance for the E.T. STRAP #6000. Classified as Device, Fixation, Tracheal Tube (product code CBH), Class I - General Controls.

Submitted by Rnd Medical Products, Inc. (Mchenry, US). The FDA issued a Cleared decision on April 28, 1983 after a review of 52 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5770 - the FDA anesthesiology and respiratory 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 Rnd Medical Products, Inc. devices

Submission Details

510(k) Number K830706 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 07, 1983
Decision Date April 28, 1983
Days to Decision 52 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
87d faster than avg
Panel avg: 139d · This submission: 52d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code CBH Device, Fixation, Tracheal Tube
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 868.5770
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.