DEROYAL INDUSTRIS, INC. BLOOD PRESSURE CUFF
K-Number: K953952 · 1995-09-28
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Device Summary
Frequently Asked Questions
What is the DEROYAL INDUSTRIS, INC. BLOOD PRESSURE CUFF?
DEROYAL INDUSTRIS, INC. BLOOD PRESSURE CUFF is a medical device that received FDA 510(k) clearance on 1995-09-28. The listed applicant is Deroyal Industries, Inc.. The 510(k) number is K953952.
When did DEROYAL INDUSTRIS, INC. BLOOD PRESSURE CUFF receive FDA 510(k) clearance?
DEROYAL INDUSTRIS, INC. BLOOD PRESSURE CUFF received FDA 510(k) clearance on 1995-09-28, under 510(k) number K953952.
Who is the listed applicant for DEROYAL INDUSTRIS, INC. BLOOD PRESSURE CUFF?
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 INDUSTRIS, INC. BLOOD PRESSURE CUFF?
The FDA product code for DEROYAL INDUSTRIS, INC. BLOOD PRESSURE CUFF is DXQ.
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: DXQ)
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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