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FDA 510(k)

DI-MIX PARENTERAL NUTRITION & MEDICINE CONTAINER

K-Number: K870274 · 1987-02-10

Decision Date1987-02-10
Product CodeKPE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DI-MIX PARENTERAL NUTRITION & MEDICINE CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is Gil-Med Industries C/O Kegan & Kegan, Ltd.. It received FDA 510(k) clearance on 1987-02-10 under 510(k) number K870274. The device is classified under product code KPE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 7 devices →

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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