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FDA 510(k)

NIKOPAD ELECTROSURGICAL GROUNDING PAD, MODEL 4777M

K-Number: K000079 · 2000-02-04

ApplicantNikomed U.S.A., Inc.
Decision Date2000-02-04
Product CodeHAM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NIKOPAD ELECTROSURGICAL GROUNDING PAD, MODEL 4777M is the device name listed in this FDA 510(k) record. The listed applicant is Nikomed U.S.A., Inc.. It received FDA 510(k) clearance on 2000-02-04 under 510(k) number K000079. The device is classified under product code HAM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NIKOPAD ELECTROSURGICAL GROUNDING PAD, MODEL 4777M?

NIKOPAD ELECTROSURGICAL GROUNDING PAD, MODEL 4777M is a medical device that received FDA 510(k) clearance on 2000-02-04. The listed applicant is Nikomed U.S.A., Inc.. The 510(k) number is K000079.

When did NIKOPAD ELECTROSURGICAL GROUNDING PAD, MODEL 4777M receive FDA 510(k) clearance?

NIKOPAD ELECTROSURGICAL GROUNDING PAD, MODEL 4777M received FDA 510(k) clearance on 2000-02-04, under 510(k) number K000079.

Who is the listed applicant for NIKOPAD ELECTROSURGICAL GROUNDING PAD, MODEL 4777M?

The FDA 510(k) record lists Nikomed U.S.A., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NIKOPAD ELECTROSURGICAL GROUNDING PAD, MODEL 4777M?

The FDA product code for NIKOPAD ELECTROSURGICAL GROUNDING PAD, MODEL 4777M is HAM.

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Related Devices (Code: HAM)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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