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FDA 510(k)

ADDITIONAL ELECTROSURGICAL GROUND PADS

K-Number: K885172 · 1989-01-06

ApplicantConmedcorp
Decision Date1989-01-06
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ADDITIONAL ELECTROSURGICAL GROUND PADS is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1989-01-06 under 510(k) number K885172. 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 ADDITIONAL ELECTROSURGICAL GROUND PADS?

ADDITIONAL ELECTROSURGICAL GROUND PADS is a medical device that received FDA 510(k) clearance on 1989-01-06. The listed applicant is Conmedcorp. The 510(k) number is K885172.

When did ADDITIONAL ELECTROSURGICAL GROUND PADS receive FDA 510(k) clearance?

ADDITIONAL ELECTROSURGICAL GROUND PADS received FDA 510(k) clearance on 1989-01-06, under 510(k) number K885172.

Who is the listed applicant for ADDITIONAL ELECTROSURGICAL GROUND PADS?

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

What is the FDA product code for ADDITIONAL ELECTROSURGICAL GROUND PADS?

The FDA product code for ADDITIONAL ELECTROSURGICAL GROUND PADS 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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