510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K000612Substantially Equivalent

Accucore Single Action Core Biopsy Device

Inrad, Kentwood MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K000612 is the FDA 510(k) clearance record for ACCUCORE SINGLE ACTION CORE BIOPSY DEVICE, a class II device, cleared for Inrad on under FDA product code KNW (Instrument, Biopsy). FDA records list 14 510(k) clearances for Inrad, from to . As of , FDA records show no recalls naming K000612.

Clearance record

Decision date
Received
(61 days to decision)
Product code
KNW Instrument, Biopsy
Regulation
21 CFR 876.1075
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Inrad 3956 44th St., SE, Kentwood MI
510(k) summary
Summary
Third party review
No

Clearances, product code KNW

Trailing 12 months
8 clearances under product code KNW in the twelve months to October 2026, August 2026 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code KNW, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20261
March 20261
April 20260
May 20261
June 20260
July 20260
August 20264
September 20260
October 20260