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FDA 510(k)

SUTTER BIPOLAR FORCEPS - SUPERGLISS

K-Number: K131012 · 2013-08-23

ApplicantSutter Medizintechnik GmbH
Decision Date2013-08-23
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUTTER BIPOLAR FORCEPS - SUPERGLISS 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 2013-08-23 under 510(k) number K131012. 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 BIPOLAR FORCEPS - SUPERGLISS?

SUTTER BIPOLAR FORCEPS - SUPERGLISS is a medical device that received FDA 510(k) clearance on 2013-08-23. The listed applicant is Sutter Medizintechnik GmbH. The 510(k) number is K131012.

When did SUTTER BIPOLAR FORCEPS - SUPERGLISS receive FDA 510(k) clearance?

SUTTER BIPOLAR FORCEPS - SUPERGLISS received FDA 510(k) clearance on 2013-08-23, under 510(k) number K131012.

Who is the listed applicant for SUTTER BIPOLAR FORCEPS - SUPERGLISS?

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 BIPOLAR FORCEPS - SUPERGLISS?

The FDA product code for SUTTER BIPOLAR FORCEPS - SUPERGLISS 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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