510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K850288Substantially Equivalent

Hepatic Parenchymal Suction Dissector

Beecher Medical Diagnostic Instrumentation, Silver Spring MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K850288 is the FDA 510(k) clearance record for HEPATIC PARENCHYMAL SUCTION DISSECTOR, a class I device, cleared for Beecher Medical Diagnostic Instrumentation on under FDA product code GDI (Dissector, Surgical, General & Plastic Surgery). FDA records list 3 510(k) clearances for Beecher Medical Diagnostic Instrumentation, from to . As of , FDA records show no recalls naming K850288.

Clearance record

Decision date
Received
(53 days to decision)
Product code
GDI Dissector, Surgical, General & Plastic Surgery
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Beecher Medical Diagnostic Instrumentation 9007 Woodland Dr., Silver Spring MD
Third party review
No

Clearances, product code GDI

Trailing 12 months

FDA records hold no clearances under product code GDI in the trailing twelve months.

FDA records show no clearances under product code GDI in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GDI, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260