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FDA 510(k)

SPECIMEN RETRIEVAL SYSTEM

K-Number: K100959 · 2010-04-22

ApplicantApplied Medical Resources
Decision Date2010-04-22
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SPECIMEN RETRIEVAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Resources. It received FDA 510(k) clearance on 2010-04-22 under 510(k) number K100959. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPECIMEN RETRIEVAL SYSTEM?

SPECIMEN RETRIEVAL SYSTEM is a medical device that received FDA 510(k) clearance on 2010-04-22. The listed applicant is Applied Medical Resources. The 510(k) number is K100959.

When did SPECIMEN RETRIEVAL SYSTEM receive FDA 510(k) clearance?

SPECIMEN RETRIEVAL SYSTEM received FDA 510(k) clearance on 2010-04-22, under 510(k) number K100959.

Who is the listed applicant for SPECIMEN RETRIEVAL SYSTEM?

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

What is the FDA product code for SPECIMEN RETRIEVAL SYSTEM?

The FDA product code for SPECIMEN RETRIEVAL SYSTEM is GCJ.

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Related Devices (Code: GCJ)

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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