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FDA 510(k)

SUTTER ELECTROSURGICAL CABLES

K-Number: K073450 · 2008-03-17

ApplicantSutter Medizintechnik GmbH
Decision Date2008-03-17
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUTTER ELECTROSURGICAL CABLES is the device name listed in this FDA 510(k) record. The listed applicant is Sutter Medizintechnik GmbH. It received FDA 510(k) clearance on 2008-03-17 under 510(k) number K073450. 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 SUTTER ELECTROSURGICAL CABLES?

SUTTER ELECTROSURGICAL CABLES is a medical device that received FDA 510(k) clearance on 2008-03-17. The listed applicant is Sutter Medizintechnik GmbH. The 510(k) number is K073450.

When did SUTTER ELECTROSURGICAL CABLES receive FDA 510(k) clearance?

SUTTER ELECTROSURGICAL CABLES received FDA 510(k) clearance on 2008-03-17, under 510(k) number K073450.

Who is the listed applicant for SUTTER ELECTROSURGICAL CABLES?

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

What is the FDA product code for SUTTER ELECTROSURGICAL CABLES?

The FDA product code for SUTTER ELECTROSURGICAL CABLES 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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