Cleared Traditional

K942466 - PROTECTAIDE CPR PROTECTION PACK NO. 17701 (FDA 510(k) Clearance)

Class II Anesthesiology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K942466 · Protectaide, Inc. · Anesthesiology device
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Oct 1994
Decision
134d
Days
Class 2
Risk

K942466 is an FDA 510(k) clearance for the PROTECTAIDE CPR PROTECTION PACK NO. 17701. Classified as Valve, Non-rebreathing (product code CBP), Class II - Special Controls.

Submitted by Protectaide, Inc. (Rockwall, US). The FDA issued a Cleared decision on October 6, 1994 after a review of 134 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 Protectaide, Inc. devices

Submission Details

510(k) Number K942466 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 25, 1994
Decision Date October 06, 1994
Days to Decision 134 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
5d faster than avg
Panel avg: 139d · This submission: 134d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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.