FDA 510(k)

NEB-U-VENT

K-Number: K872038 · 1987-08-10

Decision Date1987-08-10

Product CodeCCN

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

NEB-U-VENT is the device name listed in this FDA 510(k) record. The listed applicant is Design Technologies, Inc.. It received FDA 510(k) clearance on 1987-08-10 under 510(k) number K872038. The device is classified under product code CCN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEB-U-VENT?

NEB-U-VENT is a medical device that received FDA 510(k) clearance on 1987-08-10. The listed applicant is Design Technologies, Inc.. The 510(k) number is K872038.

When did NEB-U-VENT receive FDA 510(k) clearance?

NEB-U-VENT received FDA 510(k) clearance on 1987-08-10, under 510(k) number K872038.

Who is the listed applicant for NEB-U-VENT?

The FDA 510(k) record lists Design Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEB-U-VENT?

The FDA product code for NEB-U-VENT is CCN.

Other records listing Design Technologies, Inc. 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.

K872358STA-PUT K871262MODIFIED NOFLO I K863613NO-FLO I

Related Devices (Code: CCN)

K934945FLOWMETER NIPPLE ADAPTORCardio-Search , Ltd.K920783OXYGEN FLOW CONTROLLERPuritan Bennett Corp.K871262MODIFIED NOFLO IDesign Technologies, Inc.K863613NO-FLO IDesign Technologies, Inc.K863659FLOW INTERRUPTION INDICATORSalter Labs K863657OXYGEN CONSERVATORSalter Labs

Official Source

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