JEJUNOSTOMY SET FOR TUBE FEEDING
K-Number: K841428 · 1984-07-09
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Device Summary
Frequently Asked Questions
What is the JEJUNOSTOMY SET FOR TUBE FEEDING?
JEJUNOSTOMY SET FOR TUBE FEEDING is a medical device that received FDA 510(k) clearance on 1984-07-09. The listed applicant is Burron Medical Products, Inc.. The 510(k) number is K841428.
When did JEJUNOSTOMY SET FOR TUBE FEEDING receive FDA 510(k) clearance?
JEJUNOSTOMY SET FOR TUBE FEEDING received FDA 510(k) clearance on 1984-07-09, under 510(k) number K841428.
Who is the listed applicant for JEJUNOSTOMY SET FOR TUBE FEEDING?
The FDA 510(k) record lists Burron Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JEJUNOSTOMY SET FOR TUBE FEEDING?
The FDA product code for JEJUNOSTOMY SET FOR TUBE FEEDING 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 Burron Medical Products, Inc. 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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