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FDA 510(k)

MASTER-CHEK BOWIE-DICK TYPE TEST

K-Number: K843182 · 1984-10-09

ApplicantArvey Corp.
Decision Date1984-10-09
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MASTER-CHEK BOWIE-DICK TYPE TEST is the device name listed in this FDA 510(k) record. The listed applicant is Arvey Corp.. It received FDA 510(k) clearance on 1984-10-09 under 510(k) number K843182. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MASTER-CHEK BOWIE-DICK TYPE TEST?

MASTER-CHEK BOWIE-DICK TYPE TEST is a medical device that received FDA 510(k) clearance on 1984-10-09. The listed applicant is Arvey Corp.. The 510(k) number is K843182.

When did MASTER-CHEK BOWIE-DICK TYPE TEST receive FDA 510(k) clearance?

MASTER-CHEK BOWIE-DICK TYPE TEST received FDA 510(k) clearance on 1984-10-09, under 510(k) number K843182.

Who is the listed applicant for MASTER-CHEK BOWIE-DICK TYPE TEST?

The FDA 510(k) record lists Arvey Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MASTER-CHEK BOWIE-DICK TYPE TEST?

The FDA product code for MASTER-CHEK BOWIE-DICK TYPE TEST is JOJ.

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Other records listing Arvey Corp. as applicant

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Official Source

View on FDA Database →

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