PEDIATRIC SIZE K-TUBE A OR B
K-Number: K843939 · 1985-02-14
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Device Summary
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
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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