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FDA 510(k)

LOOP ELECTRODE, BALL ELECTRODE

K-Number: K993527 · 2000-07-06

ApplicantPalm Medical USA, Inc.
Decision Date2000-07-06
Product CodeHGI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LOOP ELECTRODE, BALL ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Palm Medical USA, Inc.. It received FDA 510(k) clearance on 2000-07-06 under 510(k) number K993527. 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 LOOP ELECTRODE, BALL ELECTRODE?

LOOP ELECTRODE, BALL ELECTRODE is a medical device that received FDA 510(k) clearance on 2000-07-06. The listed applicant is Palm Medical USA, Inc.. The 510(k) number is K993527.

When did LOOP ELECTRODE, BALL ELECTRODE receive FDA 510(k) clearance?

LOOP ELECTRODE, BALL ELECTRODE received FDA 510(k) clearance on 2000-07-06, under 510(k) number K993527.

Who is the listed applicant for LOOP ELECTRODE, BALL ELECTRODE?

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

What is the FDA product code for LOOP ELECTRODE, BALL ELECTRODE?

The FDA product code for LOOP ELECTRODE, BALL ELECTRODE is HGI.

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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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