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FDA 510(k)

Biopsy Forceps

K-Number: K252722 · 2025-09-30

ApplicantFehling Instruments GmbH
Decision Date2025-09-30
Product CodeDWZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Biopsy Forceps is the device name listed in this FDA 510(k) record. The listed applicant is Fehling Instruments GmbH. It received FDA 510(k) clearance on 2025-09-30 under 510(k) number K252722. 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 2025-09-30. The listed applicant is Fehling Instruments GmbH. The 510(k) number is K252722.

When did Biopsy Forceps receive FDA 510(k) clearance?

Biopsy Forceps received FDA 510(k) clearance on 2025-09-30, under 510(k) number K252722.

Who is the listed applicant for Biopsy Forceps?

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

What is the FDA product code for Biopsy Forceps?

The FDA product code for Biopsy Forceps is DWZ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT06824402Cryoprobe Biopsy and Chronic Rejection in Lung Transplant RecipientsRECRUITINGNCT07114783Dual-function Semirigid Thoracoscopy Versus Rigid Thoracoscopy for the Diagnosis of Pleural DiseaseNOT_YET_RECRUITINGNCT07620080EYEMAX® Versus SPYGLASS™ DS for Biliary Stricture DiagnosisNOT_YET_RECRUITINGNCT07726784Safety and Feasibility of Medical Thoracoscopy Using Single-use Flexible Bronchoscope Versus SemiRigid Pleuroscope in Pleural EffusionNOT_YET_RECRUITING

Related Devices (Code: DWZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K170726Biopsy ForcepsFehling Instruments GmbH & Co. KG

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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