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FDA 510(k)

GBI TSH NEONATAL SCREENING KIT

K-Number: K072458 · 2008-04-10

Decision Date2008-04-10
Product CodeJLW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

GBI TSH NEONATAL SCREENING KIT is the device name listed in this FDA 510(k) record. The listed applicant is Golden Bridge International, Inc.. It received FDA 510(k) clearance on 2008-04-10 under 510(k) number K072458. The device is classified under product code JLW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GBI TSH NEONATAL SCREENING KIT?

GBI TSH NEONATAL SCREENING KIT is a medical device that received FDA 510(k) clearance on 2008-04-10. The listed applicant is Golden Bridge International, Inc.. The 510(k) number is K072458.

When did GBI TSH NEONATAL SCREENING KIT receive FDA 510(k) clearance?

GBI TSH NEONATAL SCREENING KIT received FDA 510(k) clearance on 2008-04-10, under 510(k) number K072458.

Who is the listed applicant for GBI TSH NEONATAL SCREENING KIT?

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

What is the FDA product code for GBI TSH NEONATAL SCREENING KIT?

The FDA product code for GBI TSH NEONATAL SCREENING KIT is JLW.

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: JLW)

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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