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FDA 510(k)

MODIFIED NOFLO I

K-Number: K871262 · 1987-07-21

ApplicantDesign Technologies, Inc.
Decision Date1987-07-21
Product CodeCCN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODIFIED NOFLO I 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 1987-07-21 under 510(k) number K871262. 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 MODIFIED NOFLO I?

MODIFIED NOFLO I is a medical device that received FDA 510(k) clearance on 1987-07-21. The listed applicant is Design Technologies, Inc.. The 510(k) number is K871262.

When did MODIFIED NOFLO I receive FDA 510(k) clearance?

MODIFIED NOFLO I received FDA 510(k) clearance on 1987-07-21, under 510(k) number K871262.

Who is the listed applicant for MODIFIED NOFLO I?

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 MODIFIED NOFLO I?

The FDA product code for MODIFIED NOFLO I is CCN.

Related Clinical Trials

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.

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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.

K872038NEB-U-VENTK872358STA-PUTK863613NO-FLO I

Related Devices (Code: CCN)

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.

K934945FLOWMETER NIPPLE ADAPTORCardio-Search , Ltd.K920783OXYGEN FLOW CONTROLLERPuritan Bennett Corp.K872038NEB-U-VENTDesign Technologies, Inc.K863613NO-FLO IDesign Technologies, Inc.K863659FLOW INTERRUPTION INDICATORSalter LabsK863657OXYGEN 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.

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