UNIQUE NEEDLE
K-Number: K950245 · 1995-12-06
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Device Summary
Frequently Asked Questions
What is the UNIQUE NEEDLE?
UNIQUE NEEDLE is a medical device that received FDA 510(k) clearance on 1995-12-06. The listed applicant is Unique Management Ent., Inc.. The 510(k) number is K950245.
When did UNIQUE NEEDLE receive FDA 510(k) clearance?
UNIQUE NEEDLE received FDA 510(k) clearance on 1995-12-06, under 510(k) number K950245.
Who is the listed applicant for UNIQUE NEEDLE?
The FDA 510(k) record lists Unique Management Ent., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UNIQUE NEEDLE?
The FDA product code for UNIQUE NEEDLE is FMF.
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 Unique Management Ent., 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: FMF)
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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