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FDA 510(k)

ACCESS(R) TOTAL T3

K-Number: K940833 · 1994-09-07

ApplicantBio-Rad Laboratories, Inc.
Decision Date1994-09-07
Product CodeCDP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ACCESS(R) TOTAL T3 is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad Laboratories, Inc.. It received FDA 510(k) clearance on 1994-09-07 under 510(k) number K940833. The device is classified under product code CDP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCESS(R) TOTAL T3?

ACCESS(R) TOTAL T3 is a medical device that received FDA 510(k) clearance on 1994-09-07. The listed applicant is Bio-Rad Laboratories, Inc.. The 510(k) number is K940833.

When did ACCESS(R) TOTAL T3 receive FDA 510(k) clearance?

ACCESS(R) TOTAL T3 received FDA 510(k) clearance on 1994-09-07, under 510(k) number K940833.

Who is the listed applicant for ACCESS(R) TOTAL T3?

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

What is the FDA product code for ACCESS(R) TOTAL T3?

The FDA product code for ACCESS(R) TOTAL T3 is CDP.

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Related Devices (Code: CDP)

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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