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FDA 510(k)

RETURN ELECTRODE CLAMP SHELL CORD MODEL RC 201

K-Number: K982130 · 1998-08-07

ApplicantNew Deantronics, Ltd.
Decision Date1998-08-07
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RETURN ELECTRODE CLAMP SHELL CORD MODEL RC 201 is the device name listed in this FDA 510(k) record. The listed applicant is New Deantronics, Ltd.. It received FDA 510(k) clearance on 1998-08-07 under 510(k) number K982130. 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 RETURN ELECTRODE CLAMP SHELL CORD MODEL RC 201?

RETURN ELECTRODE CLAMP SHELL CORD MODEL RC 201 is a medical device that received FDA 510(k) clearance on 1998-08-07. The listed applicant is New Deantronics, Ltd.. The 510(k) number is K982130.

When did RETURN ELECTRODE CLAMP SHELL CORD MODEL RC 201 receive FDA 510(k) clearance?

RETURN ELECTRODE CLAMP SHELL CORD MODEL RC 201 received FDA 510(k) clearance on 1998-08-07, under 510(k) number K982130.

Who is the listed applicant for RETURN ELECTRODE CLAMP SHELL CORD MODEL RC 201?

The FDA 510(k) record lists New Deantronics, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RETURN ELECTRODE CLAMP SHELL CORD MODEL RC 201?

The FDA product code for RETURN ELECTRODE CLAMP SHELL CORD MODEL RC 201 is GEI.

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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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