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FDA 510(k)

FRANKLIN QUANTIC 1200

K-Number: K822236 · 1982-08-31

ApplicantBruce Franklin, Inc.
Decision Date1982-08-31
Product CodeDXK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

FRANKLIN QUANTIC 1200 is the device name listed in this FDA 510(k) record. The listed applicant is Bruce Franklin, Inc.. It received FDA 510(k) clearance on 1982-08-31 under 510(k) number K822236. The device is classified under product code DXK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FRANKLIN QUANTIC 1200?

FRANKLIN QUANTIC 1200 is a medical device that received FDA 510(k) clearance on 1982-08-31. The listed applicant is Bruce Franklin, Inc.. The 510(k) number is K822236.

When did FRANKLIN QUANTIC 1200 receive FDA 510(k) clearance?

FRANKLIN QUANTIC 1200 received FDA 510(k) clearance on 1982-08-31, under 510(k) number K822236.

Who is the listed applicant for FRANKLIN QUANTIC 1200?

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

What is the FDA product code for FRANKLIN QUANTIC 1200?

The FDA product code for FRANKLIN QUANTIC 1200 is DXK.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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