ENTERAL & NASOGASTRIC SOL. ADMIN. SET
K-Number: K800815 · 1980-07-21
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Device Summary
Frequently Asked Questions
What is the ENTERAL & NASOGASTRIC SOL. ADMIN. SET?
ENTERAL & NASOGASTRIC SOL. ADMIN. SET is a medical device that received FDA 510(k) clearance on 1980-07-21. The listed applicant is G.D. Searle and Co.. The 510(k) number is K800815.
When did ENTERAL & NASOGASTRIC SOL. ADMIN. SET receive FDA 510(k) clearance?
ENTERAL & NASOGASTRIC SOL. ADMIN. SET received FDA 510(k) clearance on 1980-07-21, under 510(k) number K800815.
Who is the listed applicant for ENTERAL & NASOGASTRIC SOL. ADMIN. SET?
The FDA 510(k) record lists G.D. Searle and Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENTERAL & NASOGASTRIC SOL. ADMIN. SET?
The FDA product code for ENTERAL & NASOGASTRIC SOL. ADMIN. SET 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 G.D. Searle and Co. 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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