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FDA 510(k)

NDM DIATEMP ELECTROSURGICAL DIS. PAD

K-Number: K801158 · 1980-05-23

ApplicantNdm Corp.
Decision Date1980-05-23
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NDM DIATEMP ELECTROSURGICAL DIS. PAD is the device name listed in this FDA 510(k) record. The listed applicant is Ndm Corp.. It received FDA 510(k) clearance on 1980-05-23 under 510(k) number K801158. 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 NDM DIATEMP ELECTROSURGICAL DIS. PAD?

NDM DIATEMP ELECTROSURGICAL DIS. PAD is a medical device that received FDA 510(k) clearance on 1980-05-23. The listed applicant is Ndm Corp.. The 510(k) number is K801158.

When did NDM DIATEMP ELECTROSURGICAL DIS. PAD receive FDA 510(k) clearance?

NDM DIATEMP ELECTROSURGICAL DIS. PAD received FDA 510(k) clearance on 1980-05-23, under 510(k) number K801158.

Who is the listed applicant for NDM DIATEMP ELECTROSURGICAL DIS. PAD?

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

What is the FDA product code for NDM DIATEMP ELECTROSURGICAL DIS. PAD?

The FDA product code for NDM DIATEMP ELECTROSURGICAL DIS. 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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