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FDA 510(k)

AD PERFECT

K-Number: K940768 · 1995-02-17

ApplicantChimera Research & Chemical, Inc.
Decision Date1995-02-17
Product CodeIFT
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

AD PERFECT 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 1995-02-17 under 510(k) number K940768. The device is classified under product code IFT. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AD PERFECT?

AD PERFECT is a medical device that received FDA 510(k) clearance on 1995-02-17. The listed applicant is Chimera Research & Chemical, Inc.. The 510(k) number is K940768.

When did AD PERFECT receive FDA 510(k) clearance?

AD PERFECT received FDA 510(k) clearance on 1995-02-17, under 510(k) number K940768.

Who is the listed applicant for AD PERFECT?

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 AD PERFECT?

The FDA product code for AD PERFECT is IFT.

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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.

K970087CR PERFECTK951877AUTOMATED ANALYSIS ASSAY FOR BILIRUBIN IN URINEK953393TOX PERFECT A TUBEK952501TOX PERFECT B TUBES AND REAGENTSK950142CR PERFECTK935408UA PERFECT

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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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