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FDA 510(k)

QBC ACCUREAD SYSTEM

K-Number: K955504 · 1996-02-05

ApplicantBecton Dickinson Diagnostic Instrument Systems
Decision Date1996-02-05
Product CodeGKZ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

QBC ACCUREAD SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Becton Dickinson Diagnostic Instrument Systems. It received FDA 510(k) clearance on 1996-02-05 under 510(k) number K955504. The device is classified under product code GKZ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QBC ACCUREAD SYSTEM?

QBC ACCUREAD SYSTEM is a medical device that received FDA 510(k) clearance on 1996-02-05. The listed applicant is Becton Dickinson Diagnostic Instrument Systems. The 510(k) number is K955504.

When did QBC ACCUREAD SYSTEM receive FDA 510(k) clearance?

QBC ACCUREAD SYSTEM received FDA 510(k) clearance on 1996-02-05, under 510(k) number K955504.

Who is the listed applicant for QBC ACCUREAD SYSTEM?

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

What is the FDA product code for QBC ACCUREAD SYSTEM?

The FDA product code for QBC ACCUREAD SYSTEM is GKZ.

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Other records listing Becton Dickinson Diagnostic Instrument Systems 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.

K954923BACTEC FUNGAL MEDIUMK954932BBL MGIT PRODUCTSK962210BACTEC 9050 SYSTEMK946268BACTEC(R) 9000TB SYSTEMK960827QBC ACCUTUBE(423406)/QBC AUTOREAD(424571)K954925BACTEC LYTIC/10 ANAEROBIC/F CULTURE VIALS

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Related Devices (Code: GKZ)

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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