DI-MIX PARENTERAL NUTRITION & MEDICINE CONTAINER
K-Number: K870274 · 1987-02-10
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Device Summary
Frequently Asked Questions
What is the DI-MIX PARENTERAL NUTRITION & MEDICINE CONTAINER?
DI-MIX PARENTERAL NUTRITION & MEDICINE CONTAINER is a medical device that received FDA 510(k) clearance on 1987-02-10. The listed applicant is Gil-Med Industries C/O Kegan & Kegan, Ltd.. The 510(k) number is K870274.
When did DI-MIX PARENTERAL NUTRITION & MEDICINE CONTAINER receive FDA 510(k) clearance?
DI-MIX PARENTERAL NUTRITION & MEDICINE CONTAINER received FDA 510(k) clearance on 1987-02-10, under 510(k) number K870274.
Who is the listed applicant for DI-MIX PARENTERAL NUTRITION & MEDICINE CONTAINER?
The FDA 510(k) record lists Gil-Med Industries C/O Kegan & Kegan, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DI-MIX PARENTERAL NUTRITION & MEDICINE CONTAINER?
The FDA product code for DI-MIX PARENTERAL NUTRITION & MEDICINE CONTAINER is KPE.
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 Gil-Med Industries C/O Kegan & Kegan, Ltd. 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: KPE)
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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