510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K152989Substantially Equivalent

Mammotome revolve Dual Vacuum Assist Biopsy System

Devicor Medical Products Inc, Cincinnati OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K152989 is the FDA 510(k) clearance record for Mammotome revolve Dual Vacuum Assist Biopsy System, a class II device, cleared for Devicor Medical Products, Inc. on under FDA product code KNW (Instrument, Biopsy). FDA records list 16 510(k) clearances for Devicor Medical Products, Inc., from to . As of , FDA records show one recall naming K152989.

Clearance record

Decision date
Received
(135 days to decision)
Product code
KNW Instrument, Biopsy
Regulation
21 CFR 876.1075
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Devicor Medical Products, Inc. 300 E-Business Way, Fifth Floor, Cincinnati OH
510(k) summary
Summary PDF
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