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FDA 510(k)

Radial Jaw 4 Pulmonary Biopsy Forceps

K-Number: K252921 · 2025-09-26

ApplicantBoston Scientific Corporation
Decision Date2025-09-26
Product CodeBWH
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

Radial Jaw 4 Pulmonary Biopsy Forceps is a medical device manufactured by Boston Scientific Corporation. It received FDA 510(k) clearance on 2025-09-26 under approval number K252921. The device is classified under product code BWH. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Radial Jaw 4 Pulmonary Biopsy Forceps?

Radial Jaw 4 Pulmonary Biopsy Forceps is a medical device that received FDA 510(k) clearance on 2025-09-26. It is manufactured by Boston Scientific Corporation. The 510(k) number is K252921.

When was Radial Jaw 4 Pulmonary Biopsy Forceps approved by the FDA?

Radial Jaw 4 Pulmonary Biopsy Forceps received FDA 510(k) clearance on 2025-09-26, under approval number K252921.

What company makes Radial Jaw 4 Pulmonary Biopsy Forceps?

Radial Jaw 4 Pulmonary Biopsy Forceps is manufactured by Boston Scientific Corporation.

What is the FDA product code for Radial Jaw 4 Pulmonary Biopsy Forceps?

The FDA product code for Radial Jaw 4 Pulmonary Biopsy Forceps is BWH.

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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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