Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

RES-Q 1, 2, 3, 4 AND 5

K-Number: K881207 · 1988-08-15

ApplicantNova-Ventrx
Decision Date1988-08-15
Product CodeBTM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RES-Q 1, 2, 3, 4 AND 5 is the device name listed in this FDA 510(k) record. The listed applicant is Nova-Ventrx. It received FDA 510(k) clearance on 1988-08-15 under 510(k) number K881207. The device is classified under product code BTM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RES-Q 1, 2, 3, 4 AND 5?

RES-Q 1, 2, 3, 4 AND 5 is a medical device that received FDA 510(k) clearance on 1988-08-15. The listed applicant is Nova-Ventrx. The 510(k) number is K881207.

When did RES-Q 1, 2, 3, 4 AND 5 receive FDA 510(k) clearance?

RES-Q 1, 2, 3, 4 AND 5 received FDA 510(k) clearance on 1988-08-15, under 510(k) number K881207.

Who is the listed applicant for RES-Q 1, 2, 3, 4 AND 5?

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 RES-Q 1, 2, 3, 4 AND 5?

The FDA product code for RES-Q 1, 2, 3, 4 AND 5 is BTM.

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 #1004K870382DRV DISP RESUSCIT 3000/BAG ADAPT 3010 & 3011K863756MODIFIED CRITERION VENTILATOR BREATHING CIRCUITK850600CO-AX VENTILATOR CIRCUIT

View all 12 devices →

Related Devices (Code: BTM)

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.

K251631The BAG manual resuscitator and accessoriesLaerdal Medical ASK243861butterflyBVMCompact Medical, Inc.K221841EOlife®ArcheonK212905Sotair DeviceSafe Bvm CorporationK210288Disposable Manual ResuscitatorXiamen Compower Medical Tech. Co., Ltd.K181583Adult Single Use Resuscitator Bag without Pressure Relief, Adult Single Use Resuscitator Bag + Pressure Relief 40CMH20, Adult Single Use Resuscitator Bag + Pressure Relief 60CMH20, Pediatric Single Use Resuscitator Bag + Pressure Relief 40CMH20, Infant Single Use Resuscitator Bag + Pressure Relief 40CMH20Flexicare Medical Limited.

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.

↑