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FDA 510(k)

PEDIATRIC SIZE K-TUBE A OR B

K-Number: K843939 · 1985-02-14

Decision Date1985-02-14
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PEDIATRIC SIZE K-TUBE A OR B 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 1985-02-14 under 510(k) number K843939. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEDIATRIC SIZE K-TUBE A OR B?

PEDIATRIC SIZE K-TUBE A OR B is a medical device that received FDA 510(k) clearance on 1985-02-14. The listed applicant is Midwest Metabolic Support Group. The 510(k) number is K843939.

When did PEDIATRIC SIZE K-TUBE A OR B receive FDA 510(k) clearance?

PEDIATRIC SIZE K-TUBE A OR B received FDA 510(k) clearance on 1985-02-14, under 510(k) number K843939.

Who is the listed applicant for PEDIATRIC SIZE K-TUBE A OR B?

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 PEDIATRIC SIZE K-TUBE A OR B?

The FDA product code for PEDIATRIC SIZE K-TUBE A OR B is KNT.

Related Clinical Trials

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.

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.

Related Devices (Code: KNT)

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.

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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