Cleared Traditional

K914471 - NEEDLECRIC

K914471 is an FDA 510(k) clearance for NEEDLECRIC, manufactured by Ajs Medical Co., Inc.. The device is a Class 2 Anesthesiology device with product code JOH cleared through the Traditional 510(k) pathway after a 265-day FDA review.

K914471 · Ajs Medical Co., Inc. · Anesthesiology device
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Jun 1992
Decision
265d
Days
Class 2
Risk

K914471 is an FDA 510(k) clearance for the NEEDLECRIC. Classified as Tube Tracheostomy And Tube Cuff (product code JOH), Class II - Special Controls.

Submitted by Ajs Medical Co., Inc. (Clarksburg, US). The FDA issued a Cleared decision on June 29, 1992 after a review of 265 days - an extended review cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5800 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Anesthesiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Ajs Medical Co., Inc. devices

FDA 510(k) Submission Details - K914471

510(k) Number K914471 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 08, 1991
Decision Date June 29, 1992
Days to Decision 265 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
125d slower than avg
Panel avg: 140d · This submission: 265d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JOH Device Classification - Class 2, Special Controls

Product Code JOH Tube Tracheostomy And Tube Cuff
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5800
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 Anesthesiology devices follow this clearance model.

Regulatory Peers - JOH Tube Tracheostomy And Tube Cuff

All 99
Devices cleared under the same product code (JOH) and FDA review panel - the closest regulatory comparables to K914471.
BIVONA HYPERFLEX TRACHEOSTOMY TUBE
K922665 · Bivona Medical Technologies · Jan 1993
BIVONA CUSTOMIZED TRACHEOSTOMY TUBES
K923878 · Bivona Medical Technologies · Dec 1992
TRACHEOSTOMY TUBE AND TUBE CUFF
K924660 · Applied Medical Resources · Dec 1992
BIVONA FOME-CUF(R) & AIR CUF(R), MODIFICATION
K913859 · Bivona Medical Technologies · Jan 1992
BIVONA AIRE-CUF(R) PEDIATRIC TRACHEOSTOMY TUBE
K914088 · Bivona Medical Technologies · Oct 1991
BIVONA CUFF MAINTENANCE DEVICE (CMD)
K914183 · Bivona Medical Technologies · Oct 1991