FDA 510(k)

LOOP/SQUARE ELECTRODE

K-Number: K952030 · 1996-07-31

Decision Date1996-07-31

Product CodeHGI

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

LOOP/SQUARE ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is E & M Engineering, Inc.. It received FDA 510(k) clearance on 1996-07-31 under 510(k) number K952030. 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/SQUARE ELECTRODE?

LOOP/SQUARE ELECTRODE is a medical device that received FDA 510(k) clearance on 1996-07-31. The listed applicant is E & M Engineering, Inc.. The 510(k) number is K952030.

When did LOOP/SQUARE ELECTRODE receive FDA 510(k) clearance?

LOOP/SQUARE ELECTRODE received FDA 510(k) clearance on 1996-07-31, under 510(k) number K952030.

Who is the listed applicant for LOOP/SQUARE ELECTRODE?

The FDA 510(k) record lists E & M Engineering, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LOOP/SQUARE ELECTRODE?

The FDA product code for LOOP/SQUARE ELECTRODE is HGI.

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Related Devices (Code: 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.