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FDA 510(k)

CLARITY

K-Number: K961670 · 1996-05-14

ApplicantSeig Technologies, Inc.
Decision Date1996-05-14
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

CLARITY is the device name listed in this FDA 510(k) record. The listed applicant is Seig Technologies, Inc.. It received FDA 510(k) clearance on 1996-05-14 under 510(k) number K961670. The device is classified under product code ESD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLARITY?

CLARITY is a medical device that received FDA 510(k) clearance on 1996-05-14. The listed applicant is Seig Technologies, Inc.. The 510(k) number is K961670.

When did CLARITY receive FDA 510(k) clearance?

CLARITY received FDA 510(k) clearance on 1996-05-14, under 510(k) number K961670.

Who is the listed applicant for CLARITY?

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

What is the FDA product code for CLARITY?

The FDA product code for CLARITY is ESD.

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Related Devices (Code: ESD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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