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FDA 510(k)

MINI GHOST, MODEL: 507

K-Number: K082524 · 2008-09-26

ApplicantNuMED, Inc.
Decision Date2008-09-26
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MINI GHOST, MODEL: 507 is the device name listed in this FDA 510(k) record. The listed applicant is NuMED, Inc.. It received FDA 510(k) clearance on 2008-09-26 under 510(k) number K082524. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINI GHOST, MODEL: 507?

MINI GHOST, MODEL: 507 is a medical device that received FDA 510(k) clearance on 2008-09-26. The listed applicant is NuMED, Inc.. The 510(k) number is K082524.

When did MINI GHOST, MODEL: 507 receive FDA 510(k) clearance?

MINI GHOST, MODEL: 507 received FDA 510(k) clearance on 2008-09-26, under 510(k) number K082524.

Who is the listed applicant for MINI GHOST, MODEL: 507?

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

What is the FDA product code for MINI GHOST, MODEL: 507?

The FDA product code for MINI GHOST, MODEL: 507 is DQY.

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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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