ALP-KII
K-Number: K810008 · 1981-01-16
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Device Summary
Frequently Asked Questions
What is the ALP-KII?
ALP-KII is a medical device that received FDA 510(k) clearance on 1981-01-16. The listed applicant is Martin'S Maine Exchange. The 510(k) number is K810008.
When did ALP-KII receive FDA 510(k) clearance?
ALP-KII received FDA 510(k) clearance on 1981-01-16, under 510(k) number K810008.
Who is the listed applicant for ALP-KII?
The FDA 510(k) record lists Martin'S Maine Exchange as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALP-KII?
The FDA product code for ALP-KII is DXQ.
Other records listing Martin'S Maine Exchange 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: DXQ)
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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