Cleared Traditional

K010191 - Y2000 POCKET RESCUE

K010191 is an FDA 510(k) clearance for Y2000 POCKET RESCUE, manufactured by Cheen Houng Ent. Co. , Ltd.. The device is a Class 2 Anesthesiology device with product code CBP cleared through the Traditional 510(k) pathway after a 51-day FDA review.

K010191 · Cheen Houng Ent. Co. , Ltd. · Anesthesiology device
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Mar 2001
Decision
51d
Days
Class 2
Risk

K010191 is an FDA 510(k) clearance for the Y2000 POCKET RESCUE. Classified as Valve, Non-rebreathing (product code CBP), Class II - Special Controls.

Submitted by Cheen Houng Ent. Co. , Ltd. (Taipei (Shulin), TW). The FDA issued a Cleared decision on March 14, 2001 after a review of 51 days - a notably fast clearance cycle.

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: 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 Cheen Houng Ent. Co. , Ltd. devices

FDA 510(k) Submission Details - K010191

510(k) Number K010191 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 22, 2001
Decision Date March 14, 2001
Days to Decision 51 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
89d faster than avg
Panel avg: 140d · This submission: 51d
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 36
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