CASABLANCA
K-Number: K841600 · 1984-11-29
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Device Summary
Frequently Asked Questions
What is the CASABLANCA?
CASABLANCA is a medical device that received FDA 510(k) clearance on 1984-11-29. The listed applicant is Arcon Corp.. The 510(k) number is K841600.
When did CASABLANCA receive FDA 510(k) clearance?
CASABLANCA received FDA 510(k) clearance on 1984-11-29, under 510(k) number K841600.
Who is the listed applicant for CASABLANCA?
The FDA 510(k) record lists Arcon Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CASABLANCA?
The FDA product code for CASABLANCA is HIS.
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 Arcon Corp. 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: HIS)
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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