Cleared Traditional

K942475 - PROTECTAIDE PERSONAL PROTECTION PACK NO. 12351

K942475 is an FDA 510(k) clearance for PROTECTAIDE PERSONAL PROTECTION PACK NO..., manufactured by Protectaide, Inc.. The device is a Class 2 General Hospital device with product code FXX cleared through the Traditional 510(k) pathway after a 146-day FDA review.

K942475 · Protectaide, Inc. · General Hospital
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Oct 1994
Decision
146d
Days
Class 2
Risk

K942475 is an FDA 510(k) clearance for the PROTECTAIDE PERSONAL PROTECTION PACK NO. 12351. Classified as Mask, Surgical (product code FXX), Class II - Special Controls.

Submitted by Protectaide, Inc. (Rockwall, US). The FDA issued a Cleared decision on October 18, 1994 after a review of 146 days - within the typical 510(k) review window.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 878.4040 - the FDA general hospital 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 General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

View all Protectaide, Inc. devices

FDA 510(k) Submission Details - K942475

510(k) Number K942475 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 25, 1994
Decision Date October 18, 1994
Days to Decision 146 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
17d slower than avg
Panel avg: 129d · This submission: 146d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FXX Device Classification - Class 2, Special Controls

Product Code FXX Mask, Surgical
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4040
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 General Hospital devices follow this clearance model.

Regulatory Peers - FXX Mask, Surgical

All 516
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