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FDA 510(k)

FLOW INTERRUPTION INDICATOR

K-Number: K863659 · 1986-10-15

ApplicantSalter Labs
Decision Date1986-10-15
Product CodeCCN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FLOW INTERRUPTION INDICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Salter Labs. It received FDA 510(k) clearance on 1986-10-15 under 510(k) number K863659. 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 FLOW INTERRUPTION INDICATOR?

FLOW INTERRUPTION INDICATOR is a medical device that received FDA 510(k) clearance on 1986-10-15. The listed applicant is Salter Labs. The 510(k) number is K863659.

When did FLOW INTERRUPTION INDICATOR receive FDA 510(k) clearance?

FLOW INTERRUPTION INDICATOR received FDA 510(k) clearance on 1986-10-15, under 510(k) number K863659.

Who is the listed applicant for FLOW INTERRUPTION INDICATOR?

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

What is the FDA product code for FLOW INTERRUPTION INDICATOR?

The FDA product code for FLOW INTERRUPTION INDICATOR is CCN.

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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.K871262MODIFIED NOFLO IDesign Technologies, Inc.K863613NO-FLO IDesign Technologies, Inc.K863657OXYGEN CONSERVATORSalter Labs

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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