DYNAFEED ENTERAL PUMP FEED BAG
K-Number: K860075 · 1986-01-23
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Device Summary
Frequently Asked Questions
What is the DYNAFEED ENTERAL PUMP FEED BAG?
DYNAFEED ENTERAL PUMP FEED BAG is a medical device that received FDA 510(k) clearance on 1986-01-23. The listed applicant is Medline Industries, Inc.. The 510(k) number is K860075.
When did DYNAFEED ENTERAL PUMP FEED BAG receive FDA 510(k) clearance?
DYNAFEED ENTERAL PUMP FEED BAG received FDA 510(k) clearance on 1986-01-23, under 510(k) number K860075.
Who is the listed applicant for DYNAFEED ENTERAL PUMP FEED BAG?
The FDA 510(k) record lists Medline Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DYNAFEED ENTERAL PUMP FEED BAG?
The FDA product code for DYNAFEED ENTERAL PUMP FEED BAG 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 Medline Industries, 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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