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FDA 510(k)

ELECTROSURGICAL UNIT

K-Number: K981781 · 1998-12-04

ApplicantHill-Med, Inc.
Decision Date1998-12-04
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTROSURGICAL UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Hill-Med, Inc.. It received FDA 510(k) clearance on 1998-12-04 under 510(k) number K981781. 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 ELECTROSURGICAL UNIT?

ELECTROSURGICAL UNIT is a medical device that received FDA 510(k) clearance on 1998-12-04. The listed applicant is Hill-Med, Inc.. The 510(k) number is K981781.

When did ELECTROSURGICAL UNIT receive FDA 510(k) clearance?

ELECTROSURGICAL UNIT received FDA 510(k) clearance on 1998-12-04, under 510(k) number K981781.

Who is the listed applicant for ELECTROSURGICAL UNIT?

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

What is the FDA product code for ELECTROSURGICAL UNIT?

The FDA product code for ELECTROSURGICAL UNIT is GEI.

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Other records listing Hill-Med, Inc. 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.

K993991HM-930 ELECTROSURGICAL UNITK961473HM-88011 SOLID STATE ELECTR SURGICAL UNITK951718HM-SPIROK940140HM-CRYOK932896HM-0690 COLPOSCOPEK932782HM-0660

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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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