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FDA 510(k)

DISPOSABLE ELECTROSURGERY GROUNDING PAD

K-Number: K984276 · 1999-02-10

ApplicantE & M Engineering, Inc.
Decision Date1999-02-10
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE ELECTROSURGERY GROUNDING PAD 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 1999-02-10 under 510(k) number K984276. 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 DISPOSABLE ELECTROSURGERY GROUNDING PAD?

DISPOSABLE ELECTROSURGERY GROUNDING PAD is a medical device that received FDA 510(k) clearance on 1999-02-10. The listed applicant is E & M Engineering, Inc.. The 510(k) number is K984276.

When did DISPOSABLE ELECTROSURGERY GROUNDING PAD receive FDA 510(k) clearance?

DISPOSABLE ELECTROSURGERY GROUNDING PAD received FDA 510(k) clearance on 1999-02-10, under 510(k) number K984276.

Who is the listed applicant for DISPOSABLE ELECTROSURGERY GROUNDING PAD?

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 DISPOSABLE ELECTROSURGERY GROUNDING PAD?

The FDA product code for DISPOSABLE ELECTROSURGERY GROUNDING PAD is GEI.

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Other records listing E & M Engineering, Inc. as applicant

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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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