DANTEC DISPOSABLE CONCENTRIC NEEDLE
K-Number: K931966 · 1994-03-30
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Device Summary
Frequently Asked Questions
What is the DANTEC DISPOSABLE CONCENTRIC NEEDLE?
DANTEC DISPOSABLE CONCENTRIC NEEDLE is a medical device that received FDA 510(k) clearance on 1994-03-30. The listed applicant is Dantec Medical, Inc.. The 510(k) number is K931966.
When did DANTEC DISPOSABLE CONCENTRIC NEEDLE receive FDA 510(k) clearance?
DANTEC DISPOSABLE CONCENTRIC NEEDLE received FDA 510(k) clearance on 1994-03-30, under 510(k) number K931966.
Who is the listed applicant for DANTEC DISPOSABLE CONCENTRIC NEEDLE?
The FDA 510(k) record lists Dantec Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DANTEC DISPOSABLE CONCENTRIC NEEDLE?
The FDA product code for DANTEC DISPOSABLE CONCENTRIC NEEDLE is IKT.
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 Dantec Medical, 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: IKT)
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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