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FDA 510(k)

PEDIATRIC REFERENCE DATABASE

K-Number: K041266 · 2004-08-11

ApplicantHologic, Inc.
Decision Date2004-08-11
Product CodeKGI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PEDIATRIC REFERENCE DATABASE is the device name listed in this FDA 510(k) record. The listed applicant is Hologic, Inc.. It received FDA 510(k) clearance on 2004-08-11 under 510(k) number K041266. The device is classified under product code KGI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEDIATRIC REFERENCE DATABASE?

PEDIATRIC REFERENCE DATABASE is a medical device that received FDA 510(k) clearance on 2004-08-11. The listed applicant is Hologic, Inc.. The 510(k) number is K041266.

When did PEDIATRIC REFERENCE DATABASE receive FDA 510(k) clearance?

PEDIATRIC REFERENCE DATABASE received FDA 510(k) clearance on 2004-08-11, under 510(k) number K041266.

Who is the listed applicant for PEDIATRIC REFERENCE DATABASE?

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

What is the FDA product code for PEDIATRIC REFERENCE DATABASE?

The FDA product code for PEDIATRIC REFERENCE DATABASE is KGI.

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Related Devices (Code: KGI)

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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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