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FDA 510(k)

TOX PERFECT B TUBES AND REAGENTS

K-Number: K952501 · 1995-08-24

Decision Date1995-08-24
Product CodeDPM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TOX PERFECT B TUBES AND REAGENTS is the device name listed in this FDA 510(k) record. The listed applicant is Chimera Research & Chemical, Inc.. It received FDA 510(k) clearance on 1995-08-24 under 510(k) number K952501. The device is classified under product code DPM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOX PERFECT B TUBES AND REAGENTS?

TOX PERFECT B TUBES AND REAGENTS is a medical device that received FDA 510(k) clearance on 1995-08-24. The listed applicant is Chimera Research & Chemical, Inc.. The 510(k) number is K952501.

When did TOX PERFECT B TUBES AND REAGENTS receive FDA 510(k) clearance?

TOX PERFECT B TUBES AND REAGENTS received FDA 510(k) clearance on 1995-08-24, under 510(k) number K952501.

Who is the listed applicant for TOX PERFECT B TUBES AND REAGENTS?

The FDA 510(k) record lists Chimera Research & Chemical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TOX PERFECT B TUBES AND REAGENTS?

The FDA product code for TOX PERFECT B TUBES AND REAGENTS is DPM.

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 Chimera Research & Chemical, 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 7 devices →

Related Devices (Code: DPM)

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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