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FDA 510(k)

VEO MULTIGAS MONITOR FOR POCKET PC, MODEL 400221

K-Number: K051857 · 2005-09-15

ApplicantWeissburg Associates
Decision Date2005-09-15
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VEO MULTIGAS MONITOR FOR POCKET PC, MODEL 400221 is the device name listed in this FDA 510(k) record. The listed applicant is Weissburg Associates. It received FDA 510(k) clearance on 2005-09-15 under 510(k) number K051857. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VEO MULTIGAS MONITOR FOR POCKET PC, MODEL 400221?

VEO MULTIGAS MONITOR FOR POCKET PC, MODEL 400221 is a medical device that received FDA 510(k) clearance on 2005-09-15. The listed applicant is Weissburg Associates. The 510(k) number is K051857.

When did VEO MULTIGAS MONITOR FOR POCKET PC, MODEL 400221 receive FDA 510(k) clearance?

VEO MULTIGAS MONITOR FOR POCKET PC, MODEL 400221 received FDA 510(k) clearance on 2005-09-15, under 510(k) number K051857.

Who is the listed applicant for VEO MULTIGAS MONITOR FOR POCKET PC, MODEL 400221?

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

What is the FDA product code for VEO MULTIGAS MONITOR FOR POCKET PC, MODEL 400221?

The FDA product code for VEO MULTIGAS MONITOR FOR POCKET PC, MODEL 400221 is CCK.

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Related Devices (Code: CCK)

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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