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FDA 510(k)

ACESSORY TO MODIFIED FREEDING JEJUNOSTO

K-Number: K813504 · 1982-01-07

ApplicantMidwest Metabolic Support Group
Decision Date1982-01-07
Product CodeKOA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ACESSORY TO MODIFIED FREEDING JEJUNOSTO is the device name listed in this FDA 510(k) record. The listed applicant is Midwest Metabolic Support Group. It received FDA 510(k) clearance on 1982-01-07 under 510(k) number K813504. The device is classified under product code KOA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACESSORY TO MODIFIED FREEDING JEJUNOSTO?

ACESSORY TO MODIFIED FREEDING JEJUNOSTO is a medical device that received FDA 510(k) clearance on 1982-01-07. The listed applicant is Midwest Metabolic Support Group. The 510(k) number is K813504.

When did ACESSORY TO MODIFIED FREEDING JEJUNOSTO receive FDA 510(k) clearance?

ACESSORY TO MODIFIED FREEDING JEJUNOSTO received FDA 510(k) clearance on 1982-01-07, under 510(k) number K813504.

Who is the listed applicant for ACESSORY TO MODIFIED FREEDING JEJUNOSTO?

The FDA 510(k) record lists Midwest Metabolic Support Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACESSORY TO MODIFIED FREEDING JEJUNOSTO?

The FDA product code for ACESSORY TO MODIFIED FREEDING JEJUNOSTO is KOA.

Related Clinical Trials

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Other records listing Midwest Metabolic Support Group 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.

K843939PEDIATRIC SIZE K-TUBE A OR BK844745K-TUBEK840019K-TUBE REPAIR KIT

Related Devices (Code: KOA)

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.

K182664FiXcisionAgency For Medical Innovations GmbHK950267URETHRAL SUTURE GUIDEApplied Medical ResourcesK932465LI VASECTOMYFemcare , Ltd.K921546VASOVASOSTOMY SETCook Urological, Inc.K931181VESITEC SUTURE PASSERVesitec Medical, Inc.K921304DDV LIGATORNorth American Medical, Inc.

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.

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