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FDA 510(k)

HM-930 ELECTROSURGICAL UNIT

K-Number: K993991 · 2000-05-30

ApplicantHill-Med, Inc.
Decision Date2000-05-30
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HM-930 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 2000-05-30 under 510(k) number K993991. 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 HM-930 ELECTROSURGICAL UNIT?

HM-930 ELECTROSURGICAL UNIT is a medical device that received FDA 510(k) clearance on 2000-05-30. The listed applicant is Hill-Med, Inc.. The 510(k) number is K993991.

When did HM-930 ELECTROSURGICAL UNIT receive FDA 510(k) clearance?

HM-930 ELECTROSURGICAL UNIT received FDA 510(k) clearance on 2000-05-30, under 510(k) number K993991.

Who is the listed applicant for HM-930 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 HM-930 ELECTROSURGICAL UNIT?

The FDA product code for HM-930 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.

K981781ELECTROSURGICAL UNITK961473HM-88011 SOLID STATE ELECTR SURGICAL UNITK951718HM-SPIROK940140HM-CRYOK932896HM-0690 COLPOSCOPEK932782HM-0660

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Related Devices (Code: GEI)

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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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