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FDA 510(k)

ADULT TDS ELECTROSURGICAL GROUNDING PAD (R.E.M.)

K-Number: K861139 · 1986-05-09

ApplicantConmedcorp
Decision Date1986-05-09
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ADULT TDS ELECTROSURGICAL GROUNDING PAD (R.E.M.) is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1986-05-09 under 510(k) number K861139. 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 ADULT TDS ELECTROSURGICAL GROUNDING PAD (R.E.M.)?

ADULT TDS ELECTROSURGICAL GROUNDING PAD (R.E.M.) is a medical device that received FDA 510(k) clearance on 1986-05-09. The listed applicant is Conmedcorp. The 510(k) number is K861139.

When did ADULT TDS ELECTROSURGICAL GROUNDING PAD (R.E.M.) receive FDA 510(k) clearance?

ADULT TDS ELECTROSURGICAL GROUNDING PAD (R.E.M.) received FDA 510(k) clearance on 1986-05-09, under 510(k) number K861139.

Who is the listed applicant for ADULT TDS ELECTROSURGICAL GROUNDING PAD (R.E.M.)?

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 ADULT TDS ELECTROSURGICAL GROUNDING PAD (R.E.M.)?

The FDA product code for ADULT TDS ELECTROSURGICAL GROUNDING PAD (R.E.M.) 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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