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FDA 510(k)

454A ELECTROSURGICAL ANALYZER

K-Number: K942627 · 1994-08-15

ApplicantHogan & Hartson
Decision Date1994-08-15
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

454A ELECTROSURGICAL ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Hogan & Hartson. It received FDA 510(k) clearance on 1994-08-15 under 510(k) number K942627. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 454A ELECTROSURGICAL ANALYZER?

454A ELECTROSURGICAL ANALYZER is a medical device that received FDA 510(k) clearance on 1994-08-15. The listed applicant is Hogan & Hartson. The 510(k) number is K942627.

When did 454A ELECTROSURGICAL ANALYZER receive FDA 510(k) clearance?

454A ELECTROSURGICAL ANALYZER received FDA 510(k) clearance on 1994-08-15, under 510(k) number K942627.

Who is the listed applicant for 454A ELECTROSURGICAL ANALYZER?

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 454A ELECTROSURGICAL ANALYZER?

The FDA product code for 454A ELECTROSURGICAL ANALYZER is GEI.

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Other records listing Hogan & Hartson as applicant

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Related Devices (Code: GEI)

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

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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