LIFESPAN 100
K-Number: K811470 · 1981-06-12
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Device Summary
Frequently Asked Questions
What is the LIFESPAN 100?
LIFESPAN 100 is a medical device that received FDA 510(k) clearance on 1981-06-12. The listed applicant is Biochem International, Inc.. The 510(k) number is K811470.
When did LIFESPAN 100 receive FDA 510(k) clearance?
LIFESPAN 100 received FDA 510(k) clearance on 1981-06-12, under 510(k) number K811470.
Who is the listed applicant for LIFESPAN 100?
The FDA 510(k) record lists Biochem International, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIFESPAN 100?
The FDA product code for LIFESPAN 100 is KLK.
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 Biochem International, 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: KLK)
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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