HYBRID NERVE LOCATION NEEDLE COATED AND UNCOATED
K-Number: K080603 · 2008-08-05
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Device Summary
Frequently Asked Questions
What is the HYBRID NERVE LOCATION NEEDLE COATED AND UNCOATED?
HYBRID NERVE LOCATION NEEDLE COATED AND UNCOATED is a medical device that received FDA 510(k) clearance on 2008-08-05. The listed applicant is Te ME NA Sas. The 510(k) number is K080603.
When did HYBRID NERVE LOCATION NEEDLE COATED AND UNCOATED receive FDA 510(k) clearance?
HYBRID NERVE LOCATION NEEDLE COATED AND UNCOATED received FDA 510(k) clearance on 2008-08-05, under 510(k) number K080603.
Who is the listed applicant for HYBRID NERVE LOCATION NEEDLE COATED AND UNCOATED?
The FDA 510(k) record lists Te ME NA Sas as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HYBRID NERVE LOCATION NEEDLE COATED AND UNCOATED?
The FDA product code for HYBRID NERVE LOCATION NEEDLE COATED AND UNCOATED is BSP.
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 Te ME NA Sas 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: BSP)
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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