SPIROX A
K-Number: K812959 · 1982-01-22
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Device Summary
Frequently Asked Questions
What is the SPIROX A?
SPIROX A is a medical device that received FDA 510(k) clearance on 1982-01-22. The listed applicant is Cairco , Ltd.. The 510(k) number is K812959.
When did SPIROX A receive FDA 510(k) clearance?
SPIROX A received FDA 510(k) clearance on 1982-01-22, under 510(k) number K812959.
Who is the listed applicant for SPIROX A?
The FDA 510(k) record lists Cairco , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SPIROX A?
The FDA product code for SPIROX A is BZK.
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 Cairco , Ltd. 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: BZK)
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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