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FDA 510(k)

ANESTHESIA INFORMATION AND DIGITAL-DRUG MANAGEMENT SYSTEM

K-Number: K062388 · 2007-02-22

ApplicantDocusys
Decision Date2007-02-22
Product CodeBSZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ANESTHESIA INFORMATION AND DIGITAL-DRUG MANAGEMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Docusys. It received FDA 510(k) clearance on 2007-02-22 under 510(k) number K062388. The device is classified under product code BSZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANESTHESIA INFORMATION AND DIGITAL-DRUG MANAGEMENT SYSTEM?

ANESTHESIA INFORMATION AND DIGITAL-DRUG MANAGEMENT SYSTEM is a medical device that received FDA 510(k) clearance on 2007-02-22. The listed applicant is Docusys. The 510(k) number is K062388.

When did ANESTHESIA INFORMATION AND DIGITAL-DRUG MANAGEMENT SYSTEM receive FDA 510(k) clearance?

ANESTHESIA INFORMATION AND DIGITAL-DRUG MANAGEMENT SYSTEM received FDA 510(k) clearance on 2007-02-22, under 510(k) number K062388.

Who is the listed applicant for ANESTHESIA INFORMATION AND DIGITAL-DRUG MANAGEMENT SYSTEM?

The FDA 510(k) record lists Docusys as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANESTHESIA INFORMATION AND DIGITAL-DRUG MANAGEMENT SYSTEM?

The FDA product code for ANESTHESIA INFORMATION AND DIGITAL-DRUG MANAGEMENT SYSTEM is BSZ.

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Related Devices (Code: BSZ)

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.

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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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