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FDA 510(k)

DISPOSABLE AND REUSABLE BALL AND LOOP ELECTRODES

K-Number: K993777 · 2000-05-25

ApplicantR-Group Intl.
Decision Date2000-05-25
Product CodeHGI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE AND REUSABLE BALL AND LOOP ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is R-Group Intl.. It received FDA 510(k) clearance on 2000-05-25 under 510(k) number K993777. 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 DISPOSABLE AND REUSABLE BALL AND LOOP ELECTRODES?

DISPOSABLE AND REUSABLE BALL AND LOOP ELECTRODES is a medical device that received FDA 510(k) clearance on 2000-05-25. The listed applicant is R-Group Intl.. The 510(k) number is K993777.

When did DISPOSABLE AND REUSABLE BALL AND LOOP ELECTRODES receive FDA 510(k) clearance?

DISPOSABLE AND REUSABLE BALL AND LOOP ELECTRODES received FDA 510(k) clearance on 2000-05-25, under 510(k) number K993777.

Who is the listed applicant for DISPOSABLE AND REUSABLE BALL AND LOOP ELECTRODES?

The FDA 510(k) record lists R-Group Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE AND REUSABLE BALL AND LOOP ELECTRODES?

The FDA product code for DISPOSABLE AND REUSABLE BALL AND LOOP 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.

Other records listing R-Group Intl. 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 7 devices →

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.

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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