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FDA 510(k)

IQ TSH IMMUNOASSAY

K-Number: K870244 · 1987-04-01

Decision Date1987-04-01
Product CodeJLW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

IQ TSH IMMUNOASSAY is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1987-04-01 under 510(k) number K870244. 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 IQ TSH IMMUNOASSAY?

IQ TSH IMMUNOASSAY is a medical device that received FDA 510(k) clearance on 1987-04-01. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K870244.

When did IQ TSH IMMUNOASSAY receive FDA 510(k) clearance?

IQ TSH IMMUNOASSAY received FDA 510(k) clearance on 1987-04-01, under 510(k) number K870244.

Who is the listed applicant for IQ TSH IMMUNOASSAY?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IQ TSH IMMUNOASSAY?

The FDA product code for IQ TSH IMMUNOASSAY 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 Bd Becton Dickinson Vacutainer Systems Preanalytic 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 632 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

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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