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FDA 510(k)

ELECTRO-SURGICAL GROUNDING PAD

K-Number: K780298 · 1978-02-28

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1978-02-28
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTRO-SURGICAL GROUNDING PAD is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1978-02-28 under 510(k) number K780298. 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 ELECTRO-SURGICAL GROUNDING PAD?

ELECTRO-SURGICAL GROUNDING PAD is a medical device that received FDA 510(k) clearance on 1978-02-28. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K780298.

When did ELECTRO-SURGICAL GROUNDING PAD receive FDA 510(k) clearance?

ELECTRO-SURGICAL GROUNDING PAD received FDA 510(k) clearance on 1978-02-28, under 510(k) number K780298.

Who is the listed applicant for ELECTRO-SURGICAL GROUNDING PAD?

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

What is the FDA product code for ELECTRO-SURGICAL GROUNDING PAD?

The FDA product code for ELECTRO-SURGICAL GROUNDING PAD is GEI.

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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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