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FDA 510(k)

QBC FIBRINOGEN

K-Number: K920258 · 1992-06-26

Decision Date1992-06-26
Product CodeKQJ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

QBC FIBRINOGEN 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 1992-06-26 under 510(k) number K920258. The device is classified under product code KQJ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QBC FIBRINOGEN?

QBC FIBRINOGEN is a medical device that received FDA 510(k) clearance on 1992-06-26. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K920258.

When did QBC FIBRINOGEN receive FDA 510(k) clearance?

QBC FIBRINOGEN received FDA 510(k) clearance on 1992-06-26, under 510(k) number K920258.

Who is the listed applicant for QBC FIBRINOGEN?

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 QBC FIBRINOGEN?

The FDA product code for QBC FIBRINOGEN is KQJ.

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: KQJ)

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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