Cleared Traditional

K892862 - FLEX-CUP PERCUSSOR

K892862 is the FDA 510(k) clearance for FLEX-CUP PERCUSSOR by Life Design Systems, Inc.. It is a Class 2 Anesthesiology device (product code BYI) cleared through the Traditional 510(k) pathway after a 37-day FDA review.

K892862 · Life Design Systems, Inc. · Anesthesiology device
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May 1989
Decision
37d
Days
Class 2
Risk

K892862 is an FDA 510(k) clearance for the FLEX-CUP PERCUSSOR. Classified as Percussor, Powered-electric (product code BYI), Class II - Special Controls.

Submitted by Life Design Systems, Inc. (Carrollton, US). The FDA issued a Cleared decision on May 25, 1989 after a review of 37 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5665 - 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 Life Design Systems, Inc. devices

Submission Details

510(k) Number K892862 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 18, 1989
Decision Date May 25, 1989
Days to Decision 37 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
103d faster than avg
Panel avg: 140d · This submission: 37d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code BYI Percussor, Powered-electric
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5665
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.