ENTERAL PUMP SET WITH ENTERAL SPIKE
K-Number: K895142 · 1990-10-02
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Device Summary
Frequently Asked Questions
What is the ENTERAL PUMP SET WITH ENTERAL SPIKE?
ENTERAL PUMP SET WITH ENTERAL SPIKE is a medical device that received FDA 510(k) clearance on 1990-10-02. The listed applicant is Delmed, Inc.. The 510(k) number is K895142.
When did ENTERAL PUMP SET WITH ENTERAL SPIKE receive FDA 510(k) clearance?
ENTERAL PUMP SET WITH ENTERAL SPIKE received FDA 510(k) clearance on 1990-10-02, under 510(k) number K895142.
Who is the listed applicant for ENTERAL PUMP SET WITH ENTERAL SPIKE?
The FDA 510(k) record lists Delmed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENTERAL PUMP SET WITH ENTERAL SPIKE?
The FDA product code for ENTERAL PUMP SET WITH ENTERAL SPIKE 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 Delmed, 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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