COBE EMERGENCY POWER SOURCE 43610-000
K-Number: K842138 · 1984-08-03
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Device Summary
Frequently Asked Questions
What is the COBE EMERGENCY POWER SOURCE 43610-000?
COBE EMERGENCY POWER SOURCE 43610-000 is a medical device that received FDA 510(k) clearance on 1984-08-03. The listed applicant is Cobe Laboratories, Inc.. The 510(k) number is K842138.
When did COBE EMERGENCY POWER SOURCE 43610-000 receive FDA 510(k) clearance?
COBE EMERGENCY POWER SOURCE 43610-000 received FDA 510(k) clearance on 1984-08-03, under 510(k) number K842138.
Who is the listed applicant for COBE EMERGENCY POWER SOURCE 43610-000?
The FDA 510(k) record lists Cobe Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COBE EMERGENCY POWER SOURCE 43610-000?
The FDA product code for COBE EMERGENCY POWER SOURCE 43610-000 is DTQ.
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 Cobe Laboratories, 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: DTQ)
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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