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FDA 510(k)

LYPHOCHEK BENZO/TCA CONTROL-SET B

K-Number: K955153 · 1996-02-05

ApplicantBio-Rad
Decision Date1996-02-05
Product CodeDIF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

LYPHOCHEK BENZO/TCA CONTROL-SET B is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1996-02-05 under 510(k) number K955153. The device is classified under product code DIF. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LYPHOCHEK BENZO/TCA CONTROL-SET B?

LYPHOCHEK BENZO/TCA CONTROL-SET B is a medical device that received FDA 510(k) clearance on 1996-02-05. The listed applicant is Bio-Rad. The 510(k) number is K955153.

When did LYPHOCHEK BENZO/TCA CONTROL-SET B receive FDA 510(k) clearance?

LYPHOCHEK BENZO/TCA CONTROL-SET B received FDA 510(k) clearance on 1996-02-05, under 510(k) number K955153.

Who is the listed applicant for LYPHOCHEK BENZO/TCA CONTROL-SET B?

The FDA 510(k) record lists Bio-Rad as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LYPHOCHEK BENZO/TCA CONTROL-SET B?

The FDA product code for LYPHOCHEK BENZO/TCA CONTROL-SET B is DIF.

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 Bio-Rad 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 319 devices →

Related Devices (Code: DIF)

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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