DEROYAL INDUSTRIES, INC TRACECART SHARPS COLLECTION CONTAINER
K-Number: K983750 · 1998-11-30
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Device Summary
Frequently Asked Questions
What is the DEROYAL INDUSTRIES, INC TRACECART SHARPS COLLECTION CONTAINER?
DEROYAL INDUSTRIES, INC TRACECART SHARPS COLLECTION CONTAINER is a medical device that received FDA 510(k) clearance on 1998-11-30. The listed applicant is Deroyal Industries, Inc.. The 510(k) number is K983750.
When did DEROYAL INDUSTRIES, INC TRACECART SHARPS COLLECTION CONTAINER receive FDA 510(k) clearance?
DEROYAL INDUSTRIES, INC TRACECART SHARPS COLLECTION CONTAINER received FDA 510(k) clearance on 1998-11-30, under 510(k) number K983750.
Who is the listed applicant for DEROYAL INDUSTRIES, INC TRACECART SHARPS COLLECTION CONTAINER?
The FDA 510(k) record lists Deroyal Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DEROYAL INDUSTRIES, INC TRACECART SHARPS COLLECTION CONTAINER?
The FDA product code for DEROYAL INDUSTRIES, INC TRACECART SHARPS COLLECTION CONTAINER 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 Deroyal Industries, 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: 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
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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