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FDA 510(k)

ANESTHESIA CONDUCTION NEEDLES

K-Number: K120475 · 2012-12-21

Decision Date2012-12-21
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ANESTHESIA CONDUCTION NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Shanghai Samedical & Plastic Instruments Co., Ltd.. It received FDA 510(k) clearance on 2012-12-21 under 510(k) number K120475. The device is classified under product code BSP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANESTHESIA CONDUCTION NEEDLES?

ANESTHESIA CONDUCTION NEEDLES is a medical device that received FDA 510(k) clearance on 2012-12-21. The listed applicant is Shanghai Samedical & Plastic Instruments Co., Ltd.. The 510(k) number is K120475.

When did ANESTHESIA CONDUCTION NEEDLES receive FDA 510(k) clearance?

ANESTHESIA CONDUCTION NEEDLES received FDA 510(k) clearance on 2012-12-21, under 510(k) number K120475.

Who is the listed applicant for ANESTHESIA CONDUCTION NEEDLES?

The FDA 510(k) record lists Shanghai Samedical & Plastic Instruments Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANESTHESIA CONDUCTION NEEDLES?

The FDA product code for ANESTHESIA CONDUCTION NEEDLES 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 Shanghai Samedical & Plastic Instruments Co., Ltd. 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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