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FDA 510(k)

TOX PERFECT A TUBE

K-Number: K953393 · 1995-10-06

ApplicantChimera Research & Chemical, Inc.
Decision Date1995-10-06
Product CodeDMP
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

TOX PERFECT A TUBE 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 1995-10-06 under 510(k) number K953393. The device is classified under product code DMP. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOX PERFECT A TUBE?

TOX PERFECT A TUBE is a medical device that received FDA 510(k) clearance on 1995-10-06. The listed applicant is Chimera Research & Chemical, Inc.. The 510(k) number is K953393.

When did TOX PERFECT A TUBE receive FDA 510(k) clearance?

TOX PERFECT A TUBE received FDA 510(k) clearance on 1995-10-06, under 510(k) number K953393.

Who is the listed applicant for TOX PERFECT A TUBE?

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 A TUBE?

The FDA product code for TOX PERFECT A TUBE is DMP.

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Other records listing Chimera Research & Chemical, Inc. as applicant

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Related Devices (Code: DMP)

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.

K973973ELECSYS CALLCHECK DIGOXINBoehringer Mannheim Corp.K780889DIGOXIN STANDARDS IN HUMAN SERUMPcl-Ria, Inc.K770411DIGI TROL TM-RX & DIGI TROL TM-TXNuclear Medical Laboratories, Inc.

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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