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FDA 510(k)

ACOH WELLNESS TESTER

K-Number: K830954 · 1983-06-10

ApplicantBradley, Campbell & Carney
Decision Date1983-06-10
Product CodeBZC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ACOH WELLNESS TESTER is the device name listed in this FDA 510(k) record. The listed applicant is Bradley, Campbell & Carney. It received FDA 510(k) clearance on 1983-06-10 under 510(k) number K830954. The device is classified under product code BZC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACOH WELLNESS TESTER?

ACOH WELLNESS TESTER is a medical device that received FDA 510(k) clearance on 1983-06-10. The listed applicant is Bradley, Campbell & Carney. The 510(k) number is K830954.

When did ACOH WELLNESS TESTER receive FDA 510(k) clearance?

ACOH WELLNESS TESTER received FDA 510(k) clearance on 1983-06-10, under 510(k) number K830954.

Who is the listed applicant for ACOH WELLNESS TESTER?

The FDA 510(k) record lists Bradley, Campbell & Carney as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACOH WELLNESS TESTER?

The FDA product code for ACOH WELLNESS TESTER is BZC.

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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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