KULTSURE
K-Number: K870231 · 1987-02-04
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Device Summary
Frequently Asked Questions
What is the KULTSURE?
KULTSURE is a medical device that received FDA 510(k) clearance on 1987-02-04. The listed applicant is Ncs Diagnostics, Inc.. The 510(k) number is K870231.
When did KULTSURE receive FDA 510(k) clearance?
KULTSURE received FDA 510(k) clearance on 1987-02-04, under 510(k) number K870231.
Who is the listed applicant for KULTSURE?
The FDA 510(k) record lists Ncs Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KULTSURE?
The FDA product code for KULTSURE is LIO.
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 Ncs Diagnostics, 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: LIO)
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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