BOYD DELIVERY UNIT
K-Number: K020833 · 2002-08-08
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Device Summary
Frequently Asked Questions
What is the BOYD DELIVERY UNIT?
BOYD DELIVERY UNIT is a medical device that received FDA 510(k) clearance on 2002-08-08. The listed applicant is Boyd Industries, Inc.. The 510(k) number is K020833.
When did BOYD DELIVERY UNIT receive FDA 510(k) clearance?
BOYD DELIVERY UNIT received FDA 510(k) clearance on 2002-08-08, under 510(k) number K020833.
Who is the listed applicant for BOYD DELIVERY UNIT?
The FDA 510(k) record lists Boyd Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BOYD DELIVERY UNIT?
The FDA product code for BOYD DELIVERY UNIT is EIA.
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 Boyd 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: EIA)
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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