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FDA 510(k)

BETA QUIK V

K-Number: K843795 · 1984-10-30

ApplicantPacific Biotech, Inc.
Decision Date1984-10-30
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BETA QUIK V is the device name listed in this FDA 510(k) record. The listed applicant is Pacific Biotech, Inc.. It received FDA 510(k) clearance on 1984-10-30 under 510(k) number K843795. The device is classified under product code JHI. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BETA QUIK V?

BETA QUIK V is a medical device that received FDA 510(k) clearance on 1984-10-30. The listed applicant is Pacific Biotech, Inc.. The 510(k) number is K843795.

When did BETA QUIK V receive FDA 510(k) clearance?

BETA QUIK V received FDA 510(k) clearance on 1984-10-30, under 510(k) number K843795.

Who is the listed applicant for BETA QUIK V?

The FDA 510(k) record lists Pacific Biotech, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BETA QUIK V?

The FDA product code for BETA QUIK V is JHI.

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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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