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FDA 510(k)

MD-6W WIRELESS CRITICAL DATA VIEWER

K-Number: K042923 · 2004-12-17

Decision Date2004-12-17
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MD-6W WIRELESS CRITICAL DATA VIEWER is the device name listed in this FDA 510(k) record. The listed applicant is The Microoptical Corporation. It received FDA 510(k) clearance on 2004-12-17 under 510(k) number K042923. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MD-6W WIRELESS CRITICAL DATA VIEWER?

MD-6W WIRELESS CRITICAL DATA VIEWER is a medical device that received FDA 510(k) clearance on 2004-12-17. The listed applicant is The Microoptical Corporation. The 510(k) number is K042923.

When did MD-6W WIRELESS CRITICAL DATA VIEWER receive FDA 510(k) clearance?

MD-6W WIRELESS CRITICAL DATA VIEWER received FDA 510(k) clearance on 2004-12-17, under 510(k) number K042923.

Who is the listed applicant for MD-6W WIRELESS CRITICAL DATA VIEWER?

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

What is the FDA product code for MD-6W WIRELESS CRITICAL DATA VIEWER?

The FDA product code for MD-6W WIRELESS CRITICAL DATA VIEWER is GCJ.

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 The Microoptical Corporation 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: GCJ)

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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