Supra Non-Stick Bipolar Forceps
K-Number: K213042 · 2022-11-17
Decision Date2022-11-17
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Supra Non-Stick Bipolar Forceps is a medical device manufactured by Guenter Bissinger Medizintechnik GmbH. It received FDA 510(k) clearance on 2022-11-17 under approval number K213042. 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 Supra Non-Stick Bipolar Forceps?
Supra Non-Stick Bipolar Forceps is a medical device that received FDA 510(k) clearance on 2022-11-17. It is manufactured by Guenter Bissinger Medizintechnik GmbH. The 510(k) number is K213042.
When was Supra Non-Stick Bipolar Forceps approved by the FDA?
Supra Non-Stick Bipolar Forceps received FDA 510(k) clearance on 2022-11-17, under approval number K213042.
What company makes Supra Non-Stick Bipolar Forceps?
Supra Non-Stick Bipolar Forceps is manufactured by Guenter Bissinger Medizintechnik GmbH.
What is the FDA product code for Supra Non-Stick Bipolar Forceps?
The FDA product code for Supra Non-Stick Bipolar Forceps 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.