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FDA 510(k)

WIDE 1MP LCD MONITOR SYSTEM

K-Number: K042634 · 2004-10-08

ApplicantWide Corporation
Decision Date2004-10-08
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

WIDE 1MP LCD MONITOR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Wide Corporation. It received FDA 510(k) clearance on 2004-10-08 under 510(k) number K042634. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WIDE 1MP LCD MONITOR SYSTEM?

WIDE 1MP LCD MONITOR SYSTEM is a medical device that received FDA 510(k) clearance on 2004-10-08. The listed applicant is Wide Corporation. The 510(k) number is K042634.

When did WIDE 1MP LCD MONITOR SYSTEM receive FDA 510(k) clearance?

WIDE 1MP LCD MONITOR SYSTEM received FDA 510(k) clearance on 2004-10-08, under 510(k) number K042634.

Who is the listed applicant for WIDE 1MP LCD MONITOR SYSTEM?

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

What is the FDA product code for WIDE 1MP LCD MONITOR SYSTEM?

The FDA product code for WIDE 1MP LCD MONITOR SYSTEM is LLZ.

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Other records listing Wide 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.

K222719CX50NK222716MX50NK222717CL24NK222722CW60NK210493CX30N (CX30PQX)K210491CW120N

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Related Devices (Code: LLZ)

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

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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