DAVIS LEAD APRON - VARIOUS CATALOGUE NUMBERS
K-Number: K912326 · 1992-03-18
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Device Summary
Frequently Asked Questions
What is the DAVIS LEAD APRON - VARIOUS CATALOGUE NUMBERS?
DAVIS LEAD APRON - VARIOUS CATALOGUE NUMBERS is a medical device that received FDA 510(k) clearance on 1992-03-18. The listed applicant is Davis Lead Aprons, Inc.. The 510(k) number is K912326.
When did DAVIS LEAD APRON - VARIOUS CATALOGUE NUMBERS receive FDA 510(k) clearance?
DAVIS LEAD APRON - VARIOUS CATALOGUE NUMBERS received FDA 510(k) clearance on 1992-03-18, under 510(k) number K912326.
Who is the listed applicant for DAVIS LEAD APRON - VARIOUS CATALOGUE NUMBERS?
The FDA 510(k) record lists Davis Lead Aprons, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DAVIS LEAD APRON - VARIOUS CATALOGUE NUMBERS?
The FDA product code for DAVIS LEAD APRON - VARIOUS CATALOGUE NUMBERS is KPY.
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 Davis Lead Aprons, 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: KPY)
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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