K-number	K252722
Device name	Biopsy Forceps
Applicant	Fehling Instruments GmbH
Product code	DWZ
Device class	Class II
Decision date	Sep 30, 2025
Decision	Substantially Equivalent
Regulation	870.4075

AI Summary

The FDA summary PDF for this submission is not available in machine-readable form — common for older clearances. View on FDA's site →

Source

View the full FDA submission: accessdata.fda.gov

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Biopsy Forceps

Everything you need for a 510(k) submission. Nothing you don't.