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FDA 510(k)

PERIPHERAL NERVE BLOCK SUPPORT TRAY

K-Number: K073187 · 2008-04-22

Decision Date2008-04-22
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PERIPHERAL NERVE BLOCK SUPPORT TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Life-Tech, Inc.. It received FDA 510(k) clearance on 2008-04-22 under 510(k) number K073187. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERIPHERAL NERVE BLOCK SUPPORT TRAY?

PERIPHERAL NERVE BLOCK SUPPORT TRAY is a medical device that received FDA 510(k) clearance on 2008-04-22. The listed applicant is Life-Tech, Inc.. The 510(k) number is K073187.

When did PERIPHERAL NERVE BLOCK SUPPORT TRAY receive FDA 510(k) clearance?

PERIPHERAL NERVE BLOCK SUPPORT TRAY received FDA 510(k) clearance on 2008-04-22, under 510(k) number K073187.

Who is the listed applicant for PERIPHERAL NERVE BLOCK SUPPORT TRAY?

The FDA 510(k) record lists Life-Tech, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERIPHERAL NERVE BLOCK SUPPORT TRAY?

The FDA product code for PERIPHERAL NERVE BLOCK SUPPORT TRAY is CAZ.

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 Life-Tech, 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.

View all 14 devices →

Related Devices (Code: CAZ)

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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