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FDA 510(k)

COMPUSPEAK

K-Number: K941566 · 1995-06-30

Decision Date1995-06-30
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COMPUSPEAK is the device name listed in this FDA 510(k) record. The listed applicant is Hogan & Hartson. It received FDA 510(k) clearance on 1995-06-30 under 510(k) number K941566. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPUSPEAK?

COMPUSPEAK is a medical device that received FDA 510(k) clearance on 1995-06-30. The listed applicant is Hogan & Hartson. The 510(k) number is K941566.

When did COMPUSPEAK receive FDA 510(k) clearance?

COMPUSPEAK received FDA 510(k) clearance on 1995-06-30, under 510(k) number K941566.

Who is the listed applicant for COMPUSPEAK?

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

What is the FDA product code for COMPUSPEAK?

The FDA product code for COMPUSPEAK is LLZ.

Related Clinical Trials

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.

Other records listing Hogan & Hartson as applicant

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.

View all 26 devices →

Related Devices (Code: LLZ)

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.

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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