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FDA 510(k)

SHARPS CONTAINER 18 GALLON

K-Number: K944121 · 1995-01-27

ApplicantBci, Inc.
Decision Date1995-01-27
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHARPS CONTAINER 18 GALLON is the device name listed in this FDA 510(k) record. The listed applicant is Bci, Inc.. It received FDA 510(k) clearance on 1995-01-27 under 510(k) number K944121. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHARPS CONTAINER 18 GALLON?

SHARPS CONTAINER 18 GALLON is a medical device that received FDA 510(k) clearance on 1995-01-27. The listed applicant is Bci, Inc.. The 510(k) number is K944121.

When did SHARPS CONTAINER 18 GALLON receive FDA 510(k) clearance?

SHARPS CONTAINER 18 GALLON received FDA 510(k) clearance on 1995-01-27, under 510(k) number K944121.

Who is the listed applicant for SHARPS CONTAINER 18 GALLON?

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

What is the FDA product code for SHARPS CONTAINER 18 GALLON?

The FDA product code for SHARPS CONTAINER 18 GALLON is FMI.

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 Bci, 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.

View all 13 devices →

Related Devices (Code: FMI)

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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