SECOND NATURE(TM)
K-Number: K871387 · 1987-05-29
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Device Summary
Frequently Asked Questions
What is the SECOND NATURE(TM)?
SECOND NATURE(TM) is a medical device that received FDA 510(k) clearance on 1987-05-29. The listed applicant is Advanced Clinical Products, Inc.. The 510(k) number is K871387.
When did SECOND NATURE(TM) receive FDA 510(k) clearance?
SECOND NATURE(TM) received FDA 510(k) clearance on 1987-05-29, under 510(k) number K871387.
Who is the listed applicant for SECOND NATURE(TM)?
The FDA 510(k) record lists Advanced Clinical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SECOND NATURE(TM)?
The FDA product code for SECOND NATURE(TM) is KNX.
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 Advanced Clinical 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: KNX)
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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