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FDA 510(k)

PEDIATRIC INGESTASCAN

K-Number: K003305 · 2000-12-22

Decision Date2000-12-22
Product CodeHPM
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PEDIATRIC INGESTASCAN is the device name listed in this FDA 510(k) record. The listed applicant is Adams Electronics, Inc.. It received FDA 510(k) clearance on 2000-12-22 under 510(k) number K003305. The device is classified under product code HPM. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEDIATRIC INGESTASCAN?

PEDIATRIC INGESTASCAN is a medical device that received FDA 510(k) clearance on 2000-12-22. The listed applicant is Adams Electronics, Inc.. The 510(k) number is K003305.

When did PEDIATRIC INGESTASCAN receive FDA 510(k) clearance?

PEDIATRIC INGESTASCAN received FDA 510(k) clearance on 2000-12-22, under 510(k) number K003305.

Who is the listed applicant for PEDIATRIC INGESTASCAN?

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

What is the FDA product code for PEDIATRIC INGESTASCAN?

The FDA product code for PEDIATRIC INGESTASCAN is HPM.

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.

Related Devices (Code: HPM)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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