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FDA 510(k)

GI BLEEDER/OD SET

K-Number: K913476 · 1992-02-12

ApplicantIcu Medical, Inc.
Decision Date1992-02-12
Product CodeKNT
Advisory CommitteeGU
DecisionUnknown

Device Summary

GI BLEEDER/OD SET 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 1992-02-12 under 510(k) number K913476. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the GI BLEEDER/OD SET?

GI BLEEDER/OD SET is a medical device that received FDA 510(k) clearance on 1992-02-12. The listed applicant is Icu Medical, Inc.. The 510(k) number is K913476.

When did GI BLEEDER/OD SET receive FDA 510(k) clearance?

GI BLEEDER/OD SET received FDA 510(k) clearance on 1992-02-12, under 510(k) number K913476.

Who is the listed applicant for GI BLEEDER/OD SET?

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 GI BLEEDER/OD SET?

The FDA product code for GI BLEEDER/OD SET is KNT.

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Related Devices (Code: KNT)

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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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