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FDA 510(k)

DRV DISP RESUSCIT 3000/BAG ADAPT 3010 & 3011

K-Number: K870382 · 1987-03-06

ApplicantNova-Ventrx
Decision Date1987-03-06
Product CodeCBP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DRV DISP RESUSCIT 3000/BAG ADAPT 3010 & 3011 is the device name listed in this FDA 510(k) record. The listed applicant is Nova-Ventrx. It received FDA 510(k) clearance on 1987-03-06 under 510(k) number K870382. The device is classified under product code CBP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRV DISP RESUSCIT 3000/BAG ADAPT 3010 & 3011?

DRV DISP RESUSCIT 3000/BAG ADAPT 3010 & 3011 is a medical device that received FDA 510(k) clearance on 1987-03-06. The listed applicant is Nova-Ventrx. The 510(k) number is K870382.

When did DRV DISP RESUSCIT 3000/BAG ADAPT 3010 & 3011 receive FDA 510(k) clearance?

DRV DISP RESUSCIT 3000/BAG ADAPT 3010 & 3011 received FDA 510(k) clearance on 1987-03-06, under 510(k) number K870382.

Who is the listed applicant for DRV DISP RESUSCIT 3000/BAG ADAPT 3010 & 3011?

The FDA 510(k) record lists Nova-Ventrx as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DRV DISP RESUSCIT 3000/BAG ADAPT 3010 & 3011?

The FDA product code for DRV DISP RESUSCIT 3000/BAG ADAPT 3010 & 3011 is CBP.

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Other records listing Nova-Ventrx as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K952267CRITERION, CRITERION I.V., MODIFIEDK954480CONDENSATE COLLECTION KITK893760CRITERION I.V. VENTILATOR BREATHING CIRCUIT #1004K881207RES-Q 1, 2, 3, 4 AND 5K863756MODIFIED CRITERION VENTILATOR BREATHING CIRCUITK850600CO-AX VENTILATOR CIRCUIT

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Related Devices (Code: CBP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K241366QualityFlow O2 Series (QualityFLOW O2); QualityFlow O2 Series (QualityFLOW O2 MTV)Dehas Medical Systems GmbHK234053F&P Optiflow Flow DiverterFisher & Paykel Healthcare, Ltd.K210992Altech® Exhalation Valve (Single Limb and Dual Limb)Meditera Tibbi Malzeme San VE Tic ASK192285CPR Face ShieldFirstar Healthcare Company Limited (Guangzhou)K173770OJR215 Pressure Relief ManifoldFisher & Paykel Healthcare LimitedK171961Compower CPR Mask With Oxygen Port, Compower CPR Mask Without Oxygen Port, Compower Infant CPR Mask, Compower Non-Rebreathing Valve (22mm/15mmOD), Non-Rebreathing Valve (22mm/18.5mm)Xiamen Compower Medical Tech. Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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