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FDA 510(k)

BAXTER ONE GALLON SHARPS DISPOSAL CONTAINERS

K-Number: K943594 · 1994-08-17

Decision Date1994-08-17
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BAXTER ONE GALLON SHARPS DISPOSAL CONTAINERS is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1994-08-17 under 510(k) number K943594. 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 BAXTER ONE GALLON SHARPS DISPOSAL CONTAINERS?

BAXTER ONE GALLON SHARPS DISPOSAL CONTAINERS is a medical device that received FDA 510(k) clearance on 1994-08-17. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K943594.

When did BAXTER ONE GALLON SHARPS DISPOSAL CONTAINERS receive FDA 510(k) clearance?

BAXTER ONE GALLON SHARPS DISPOSAL CONTAINERS received FDA 510(k) clearance on 1994-08-17, under 510(k) number K943594.

Who is the listed applicant for BAXTER ONE GALLON SHARPS DISPOSAL CONTAINERS?

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

What is the FDA product code for BAXTER ONE GALLON SHARPS DISPOSAL CONTAINERS?

The FDA product code for BAXTER ONE GALLON SHARPS DISPOSAL CONTAINERS 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 Baxter Healthcare 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 504 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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