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FDA 510(k)

SOLACE POST-OPERATIVE PAIN RELIEF INFUSION SYSTEM

K-Number: K060933 · 2006-05-09

Decision Date2006-05-09
Product CodeMEB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SOLACE POST-OPERATIVE PAIN RELIEF INFUSION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Apex Medical Technologies, Inc.. It received FDA 510(k) clearance on 2006-05-09 under 510(k) number K060933. The device is classified under product code MEB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOLACE POST-OPERATIVE PAIN RELIEF INFUSION SYSTEM?

SOLACE POST-OPERATIVE PAIN RELIEF INFUSION SYSTEM is a medical device that received FDA 510(k) clearance on 2006-05-09. The listed applicant is Apex Medical Technologies, Inc.. The 510(k) number is K060933.

When did SOLACE POST-OPERATIVE PAIN RELIEF INFUSION SYSTEM receive FDA 510(k) clearance?

SOLACE POST-OPERATIVE PAIN RELIEF INFUSION SYSTEM received FDA 510(k) clearance on 2006-05-09, under 510(k) number K060933.

Who is the listed applicant for SOLACE POST-OPERATIVE PAIN RELIEF INFUSION SYSTEM?

The FDA 510(k) record lists Apex Medical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SOLACE POST-OPERATIVE PAIN RELIEF INFUSION SYSTEM?

The FDA product code for SOLACE POST-OPERATIVE PAIN RELIEF INFUSION SYSTEM is MEB.

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 Apex Medical Technologies, 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 8 devices →

Related Devices (Code: MEB)

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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