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FDA 510(k)

CHURCHILL PARENTERAL NUTRITION BAG - EVA

K-Number: K870395 · 1987-10-15

Decision Date1987-10-15
Product CodeKPE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CHURCHILL PARENTERAL NUTRITION BAG - EVA is the device name listed in this FDA 510(k) record. The listed applicant is Churchill Corp.. It received FDA 510(k) clearance on 1987-10-15 under 510(k) number K870395. 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 CHURCHILL PARENTERAL NUTRITION BAG - EVA?

CHURCHILL PARENTERAL NUTRITION BAG - EVA is a medical device that received FDA 510(k) clearance on 1987-10-15. The listed applicant is Churchill Corp.. The 510(k) number is K870395.

When did CHURCHILL PARENTERAL NUTRITION BAG - EVA receive FDA 510(k) clearance?

CHURCHILL PARENTERAL NUTRITION BAG - EVA received FDA 510(k) clearance on 1987-10-15, under 510(k) number K870395.

Who is the listed applicant for CHURCHILL PARENTERAL NUTRITION BAG - EVA?

The FDA 510(k) record lists Churchill Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHURCHILL PARENTERAL NUTRITION BAG - EVA?

The FDA product code for CHURCHILL PARENTERAL NUTRITION BAG - EVA 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 Churchill Corp. 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 35 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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