CPR PLUS
K-Number: K926333 · 1993-11-08
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Device Summary
Frequently Asked Questions
What is the CPR PLUS?
CPR PLUS is a medical device that received FDA 510(k) clearance on 1993-11-08. The listed applicant is Kells Medical, Inc.. The 510(k) number is K926333.
When did CPR PLUS receive FDA 510(k) clearance?
CPR PLUS received FDA 510(k) clearance on 1993-11-08, under 510(k) number K926333.
Who is the listed applicant for CPR PLUS?
The FDA 510(k) record lists Kells Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CPR PLUS?
The FDA product code for CPR PLUS is LIX.
Other records listing Kells 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: LIX)
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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