Cleared Traditional

K001742 - RESUSCI INFLATE-A-SHIELD CPR BARRIER

K001742 is an FDA 510(k) clearance for RESUSCI INFLATE-A-SHIELD CPR BARRIER, manufactured by Laerdal Medical Corp.. The device is a Class 2 Anesthesiology device with product code CBP cleared through the Traditional 510(k) pathway after a 120-day FDA review.

K001742 · Laerdal Medical Corp. · Anesthesiology device
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Oct 2000
Decision
120d
Days
Class 2
Risk

K001742 is an FDA 510(k) clearance for the RESUSCI INFLATE-A-SHIELD CPR BARRIER. Classified as Valve, Non-rebreathing (product code CBP), Class II - Special Controls.

Submitted by Laerdal Medical Corp. (North Attleboro, US). The FDA issued a Cleared decision on October 6, 2000 after a review of 120 days - within the typical 510(k) review window.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5870 - 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 Laerdal Medical Corp. devices

FDA 510(k) Submission Details - K001742

510(k) Number K001742 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 08, 2000
Decision Date October 06, 2000
Days to Decision 120 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
20d faster than avg
Panel avg: 140d · This submission: 120d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

CBP Device Classification - Class 2, Special Controls

Product Code CBP Valve, Non-rebreathing
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5870
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 - CBP Valve, Non-rebreathing

All 63
Devices cleared under the same product code (CBP) and FDA review panel - the closest regulatory comparables to K001742.
PRESSURE MANIFOLD, MODEL BC 110
K040366 · Fisher &Paykel Healthcare , Ltd. · Mar 2004
MODIFICATION TO HIOX
K030943 · Sensor Medics Corp. · Apr 2003
HI-OX
K020665 · Sensor Medics Corp. · Jul 2002
RUSCH EMERGENCY MASK
K993528 · Rusch, Inc. · May 2000
FACE-2-FACE CPR PROTECTION SHIELD
K991617 · Whiteline Plastics, Inc. · Nov 1999
AUTO-PEEP MEASUREMENT DEVICE, MODEL # KC 9-P
K983631 · Instrumentation Industries, Inc. · Jul 1999