Biopsy Forceps
K-Number: K170726 · 2017-06-02
ApplicantFehling Instruments GmbH & Co. KG
Decision Date2017-06-02
Product CodeDWZ
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Biopsy Forceps is a medical device manufactured by Fehling Instruments GmbH & Co. KG. It received FDA 510(k) clearance on 2017-06-02 under approval number K170726. The device is classified under product code DWZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Biopsy Forceps?
Biopsy Forceps is a medical device that received FDA 510(k) clearance on 2017-06-02. It is manufactured by Fehling Instruments GmbH & Co. KG. The 510(k) number is K170726.
When was Biopsy Forceps approved by the FDA?
Biopsy Forceps received FDA 510(k) clearance on 2017-06-02, under approval number K170726.
What company makes Biopsy Forceps?
Biopsy Forceps is manufactured by Fehling Instruments GmbH & Co. KG.
What is the FDA product code for Biopsy Forceps?
The FDA product code for Biopsy Forceps is DWZ.
Related Clinical Trials
Other Devices by Fehling Instruments GmbH & Co. KG
Related Devices (Code: DWZ)
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.