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FDA 510(k)

EMPTY I.V. CONTAINER

K-Number: K910936 · 1991-07-16

Decision Date1991-07-16
Product CodeKPE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EMPTY I.V. CONTAINER is the device name listed in this FDA 510(k) record. The listed applicant is Ellis Pharmaceutical Consulting, Inc.. It received FDA 510(k) clearance on 1991-07-16 under 510(k) number K910936. 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 EMPTY I.V. CONTAINER?

EMPTY I.V. CONTAINER is a medical device that received FDA 510(k) clearance on 1991-07-16. The listed applicant is Ellis Pharmaceutical Consulting, Inc.. The 510(k) number is K910936.

When did EMPTY I.V. CONTAINER receive FDA 510(k) clearance?

EMPTY I.V. CONTAINER received FDA 510(k) clearance on 1991-07-16, under 510(k) number K910936.

Who is the listed applicant for EMPTY I.V. CONTAINER?

The FDA 510(k) record lists Ellis Pharmaceutical Consulting, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EMPTY I.V. CONTAINER?

The FDA product code for EMPTY I.V. 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 Ellis Pharmaceutical Consulting, 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: 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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