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FDA 510(k)

HYPERGRAPH

K-Number: K941162 · 1994-12-15

ApplicantDermed Diagnostics, Inc.
Decision Date1994-12-15
Product CodeDSB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HYPERGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Dermed Diagnostics, Inc.. It received FDA 510(k) clearance on 1994-12-15 under 510(k) number K941162. The device is classified under product code DSB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYPERGRAPH?

HYPERGRAPH is a medical device that received FDA 510(k) clearance on 1994-12-15. The listed applicant is Dermed Diagnostics, Inc.. The 510(k) number is K941162.

When did HYPERGRAPH receive FDA 510(k) clearance?

HYPERGRAPH received FDA 510(k) clearance on 1994-12-15, under 510(k) number K941162.

Who is the listed applicant for HYPERGRAPH?

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

What is the FDA product code for HYPERGRAPH?

The FDA product code for HYPERGRAPH is DSB.

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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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