H-3000 OXYGEN CONCENTRATOR
K-Number: K890150 · 1989-01-31
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Device Summary
Frequently Asked Questions
What is the H-3000 OXYGEN CONCENTRATOR?
H-3000 OXYGEN CONCENTRATOR is a medical device that received FDA 510(k) clearance on 1989-01-31. The listed applicant is Healthdyne, Inc.. The 510(k) number is K890150.
When did H-3000 OXYGEN CONCENTRATOR receive FDA 510(k) clearance?
H-3000 OXYGEN CONCENTRATOR received FDA 510(k) clearance on 1989-01-31, under 510(k) number K890150.
Who is the listed applicant for H-3000 OXYGEN CONCENTRATOR?
The FDA 510(k) record lists Healthdyne, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for H-3000 OXYGEN CONCENTRATOR?
The FDA product code for H-3000 OXYGEN CONCENTRATOR is CAW.
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 Healthdyne, 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: CAW)
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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