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FDA 510(k)

IMMUCHEM NEONATAL TSH-MP ELISA

K-Number: K913963 · 1991-12-13

Decision Date1991-12-13
Product CodeJLW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

IMMUCHEM NEONATAL TSH-MP ELISA is the device name listed in this FDA 510(k) record. The listed applicant is Icn Biomedicals, Inc.. It received FDA 510(k) clearance on 1991-12-13 under 510(k) number K913963. 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 IMMUCHEM NEONATAL TSH-MP ELISA?

IMMUCHEM NEONATAL TSH-MP ELISA is a medical device that received FDA 510(k) clearance on 1991-12-13. The listed applicant is Icn Biomedicals, Inc.. The 510(k) number is K913963.

When did IMMUCHEM NEONATAL TSH-MP ELISA receive FDA 510(k) clearance?

IMMUCHEM NEONATAL TSH-MP ELISA received FDA 510(k) clearance on 1991-12-13, under 510(k) number K913963.

Who is the listed applicant for IMMUCHEM NEONATAL TSH-MP ELISA?

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

What is the FDA product code for IMMUCHEM NEONATAL TSH-MP ELISA?

The FDA product code for IMMUCHEM NEONATAL TSH-MP ELISA 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.

Other records listing Icn Biomedicals, Inc. as applicant

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.

View all 11 devices →

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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