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FDA 510(k)

THOMAS MEDICAL ELECTRODES

K-Number: K022593 · 2002-11-01

ApplicantThomas Medical, Inc.
Decision Date2002-11-01
Product CodeHGI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

THOMAS MEDICAL ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is Thomas Medical, Inc.. It received FDA 510(k) clearance on 2002-11-01 under 510(k) number K022593. The device is classified under product code HGI. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THOMAS MEDICAL ELECTRODES?

THOMAS MEDICAL ELECTRODES is a medical device that received FDA 510(k) clearance on 2002-11-01. The listed applicant is Thomas Medical, Inc.. The 510(k) number is K022593.

When did THOMAS MEDICAL ELECTRODES receive FDA 510(k) clearance?

THOMAS MEDICAL ELECTRODES received FDA 510(k) clearance on 2002-11-01, under 510(k) number K022593.

Who is the listed applicant for THOMAS MEDICAL ELECTRODES?

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

What is the FDA product code for THOMAS MEDICAL ELECTRODES?

The FDA product code for THOMAS MEDICAL ELECTRODES is HGI.

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.

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Other records listing Thomas Medical, 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.

K022503UTERINE INJECTOR

Related Devices (Code: HGI)

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.

K202915IRIS Thermocoagulator and Digital ColposcopeLiger Medical, LLCK152843Liger Medical HTU-110Liger Medical, LLCK121881DOMAIN SURGICAL SYSTEMDomain Surgical, Inc.K070877ENDOCERVICAL ELECTRODE # 2Modern Medical Equipment Mfg., Ltd.K061651FISCHER CONE BIOPSY EXCISOR, MODELS 900-150, 151, 152, 154, 155, 157 AND 158Apple Medical Corp.K003608SOVEREIGN BIPOLAR INSTRUMENTS FOR GYNECOLOGYAesculap, Inc.

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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