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FDA 510(k)

LOPEZ VALVE WITH NG SUMP TUBE

K-Number: K921104 · 1992-10-26

ApplicantIcu Medical, Inc.
Decision Date1992-10-26
Product CodeFEG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LOPEZ VALVE WITH NG SUMP TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Icu Medical, Inc.. It received FDA 510(k) clearance on 1992-10-26 under 510(k) number K921104. The device is classified under product code FEG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOPEZ VALVE WITH NG SUMP TUBE?

LOPEZ VALVE WITH NG SUMP TUBE is a medical device that received FDA 510(k) clearance on 1992-10-26. The listed applicant is Icu Medical, Inc.. The 510(k) number is K921104.

When did LOPEZ VALVE WITH NG SUMP TUBE receive FDA 510(k) clearance?

LOPEZ VALVE WITH NG SUMP TUBE received FDA 510(k) clearance on 1992-10-26, under 510(k) number K921104.

Who is the listed applicant for LOPEZ VALVE WITH NG SUMP TUBE?

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

What is the FDA product code for LOPEZ VALVE WITH NG SUMP TUBE?

The FDA product code for LOPEZ VALVE WITH NG SUMP TUBE is FEG.

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Related Devices (Code: FEG)

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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