FDA 510(k)

NO-FLO I

K-Number: K863613 · 1986-12-15

Decision Date1986-12-15

Product CodeCCN

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

NO-FLO 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 1986-12-15 under 510(k) number K863613. 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 NO-FLO I?

NO-FLO I is a medical device that received FDA 510(k) clearance on 1986-12-15. The listed applicant is Design Technologies, Inc.. The 510(k) number is K863613.

When did NO-FLO I receive FDA 510(k) clearance?

NO-FLO I received FDA 510(k) clearance on 1986-12-15, under 510(k) number K863613.

Who is the listed applicant for NO-FLO 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 NO-FLO I?

The FDA product code for NO-FLO I 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.

K872038NEB-U-VENT K872358STA-PUT K871262MODIFIED NOFLO I

Related Devices (Code: CCN)

K934945FLOWMETER NIPPLE ADAPTORCardio-Search , Ltd.K920783OXYGEN FLOW CONTROLLERPuritan Bennett Corp.K872038NEB-U-VENTDesign Technologies, Inc.K871262MODIFIED NOFLO 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.