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FDA 510(k)

ARNCO I.V. MONITOR

K-Number: K760694 · 1976-12-23

ApplicantA.R. Nelson Co., Inc.
Decision Date1976-12-23
Product CodeFLN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ARNCO I.V. MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is A.R. Nelson Co., Inc.. It received FDA 510(k) clearance on 1976-12-23 under 510(k) number K760694. The device is classified under product code FLN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARNCO I.V. MONITOR?

ARNCO I.V. MONITOR is a medical device that received FDA 510(k) clearance on 1976-12-23. The listed applicant is A.R. Nelson Co., Inc.. The 510(k) number is K760694.

When did ARNCO I.V. MONITOR receive FDA 510(k) clearance?

ARNCO I.V. MONITOR received FDA 510(k) clearance on 1976-12-23, under 510(k) number K760694.

Who is the listed applicant for ARNCO I.V. MONITOR?

The FDA 510(k) record lists A.R. Nelson Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARNCO I.V. MONITOR?

The FDA product code for ARNCO I.V. MONITOR is FLN.

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Related Devices (Code: FLN)

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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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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