BLOOD PRESSURE SLEEVE W/TUBING
K-Number: K874233 · 1988-03-22
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Device Summary
Frequently Asked Questions
What is the BLOOD PRESSURE SLEEVE W/TUBING?
BLOOD PRESSURE SLEEVE W/TUBING is a medical device that received FDA 510(k) clearance on 1988-03-22. The listed applicant is Devcom, Inc.. The 510(k) number is K874233.
When did BLOOD PRESSURE SLEEVE W/TUBING receive FDA 510(k) clearance?
BLOOD PRESSURE SLEEVE W/TUBING received FDA 510(k) clearance on 1988-03-22, under 510(k) number K874233.
Who is the listed applicant for BLOOD PRESSURE SLEEVE W/TUBING?
The FDA 510(k) record lists Devcom, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BLOOD PRESSURE SLEEVE W/TUBING?
The FDA product code for BLOOD PRESSURE SLEEVE W/TUBING 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 Devcom, 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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