Cleared Traditional

K870382 - DRV DISP RESUSCIT 3000/BAG ADAPT 3010 & 3011

K870382 is an FDA 510(k) clearance for DRV DISP RESUSCIT 3000/BAG ADAPT 3010 &..., manufactured by Nova-Ventrx. The device is a Class 2 Anesthesiology device with product code CBP cleared through the Traditional 510(k) pathway after a 36-day FDA review.

K870382 · Nova-Ventrx · Anesthesiology device
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Mar 1987
Decision
36d
Days
Class 2
Risk

K870382 is an FDA 510(k) clearance for the DRV DISP RESUSCIT 3000/BAG ADAPT 3010 & 3011. Classified as Valve, Non-rebreathing (product code CBP), Class II - Special Controls.

Submitted by Nova-Ventrx (Wheeling, US). The FDA issued a Cleared decision on March 6, 1987 after a review of 36 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 Nova-Ventrx devices

FDA 510(k) Submission Details - K870382

510(k) Number K870382 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 29, 1987
Decision Date March 06, 1987
Days to Decision 36 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
104d faster than avg
Panel avg: 140d · This submission: 36d
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 63
Devices cleared under the same product code (CBP) and FDA review panel - the closest regulatory comparables to K870382.
NO. 1552, VALVED VENTI-COMP
K870895 · Hudson Oxygen Therapy Sales Co. · May 1987
1160 SIMPLE ISOLATION VALVE & 1161 FILTERED VALVE
K870138 · Hudson Oxygen Therapy Sales Co. · Mar 1987
INSPIRON(R) BREATH FOR LIFE EMERG. RESUSCITATOR
K870253 · Intertech Resources, Inc. · Mar 1987
RESCUE VALVE
K833748 · Respironics, Inc. · Dec 1983
RESUSCITATION VALVE
K832868 · Boehringer Laboratories · Sep 1983
WHISTLER IN-LINE PRESSURE RELEASE VALVE
K831246 · Airlife, Inc. · Jul 1983