Cleared Traditional

K000314 - INCENTIVE SPIROMETER

K000314 is an FDA 510(k) clearance for INCENTIVE SPIROMETER, manufactured by Engineered Medical Systems. The device is a Class 2 Anesthesiology device with product code BWF cleared through the Traditional 510(k) pathway after a 71-day FDA review.

K000314 · Engineered Medical Systems · Anesthesiology device
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Apr 2000
Decision
71d
Days
Class 2
Risk

K000314 is an FDA 510(k) clearance for the INCENTIVE SPIROMETER. Classified as Spirometer, Therapeutic (incentive) (product code BWF), Class II - Special Controls.

Submitted by Engineered Medical Systems (Indianapolis, US). The FDA issued a Cleared decision on April 12, 2000 after a review of 71 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5690 - 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 Engineered Medical Systems devices

FDA 510(k) Submission Details - K000314

510(k) Number K000314 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 01, 2000
Decision Date April 12, 2000
Days to Decision 71 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
69d faster than avg
Panel avg: 140d · This submission: 71d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

BWF Device Classification - Class 2, Special Controls

Product Code BWF Spirometer, Therapeutic (incentive)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5690
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 - BWF Spirometer, Therapeutic (incentive)

All 37
Devices cleared under the same product code (BWF) and FDA review panel - the closest regulatory comparables to K000314.
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