ARVEE APNEA MONITOR, MODEL 4800
K-Number: K900730 · 1990-06-14
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Device Summary
Frequently Asked Questions
What is the ARVEE APNEA MONITOR, MODEL 4800?
ARVEE APNEA MONITOR, MODEL 4800 is a medical device that received FDA 510(k) clearance on 1990-06-14. The listed applicant is Arvee Medical, Inc.. The 510(k) number is K900730.
When did ARVEE APNEA MONITOR, MODEL 4800 receive FDA 510(k) clearance?
ARVEE APNEA MONITOR, MODEL 4800 received FDA 510(k) clearance on 1990-06-14, under 510(k) number K900730.
Who is the listed applicant for ARVEE APNEA MONITOR, MODEL 4800?
The FDA 510(k) record lists Arvee Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARVEE APNEA MONITOR, MODEL 4800?
The FDA product code for ARVEE APNEA MONITOR, MODEL 4800 is BZQ.
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 Arvee Medical, 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: BZQ)
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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