510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K994272Substantially Equivalent

Automated Core Biopsy Device

Promex, Inc., Franklin IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K994272 is the FDA 510(k) clearance record for AUTOMATED CORE BIOPSY DEVICE, a class II device, cleared for Promex, Inc. on under FDA product code KNW (Instrument, Biopsy). FDA records list 18 510(k) clearances for Promex, Inc., from to . As of , FDA records show no recalls naming K994272.

Clearance record

Decision date
Received
(18 days to decision)
Product code
KNW Instrument, Biopsy
Regulation
21 CFR 876.1075
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Promex, Inc. 3049 Hudson St., Franklin IN
510(k) summary
Statement
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