KM-KAL L3
K-Number: K823044 · 1982-12-09
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Device Summary
Frequently Asked Questions
What is the KM-KAL L3?
KM-KAL L3 is a medical device that received FDA 510(k) clearance on 1982-12-09. The listed applicant is Kmn Products, Inc.. The 510(k) number is K823044.
When did KM-KAL L3 receive FDA 510(k) clearance?
KM-KAL L3 received FDA 510(k) clearance on 1982-12-09, under 510(k) number K823044.
Who is the listed applicant for KM-KAL L3?
The FDA 510(k) record lists Kmn Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KM-KAL L3?
The FDA product code for KM-KAL L3 is JIX.
Other records listing Kmn Products, 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: JIX)
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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