510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K960004Substantially Equivalent

Cell Recovery System

Medical Device Technologies, Inc., San Diego CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K960004 is the FDA 510(k) clearance record for CELL RECOVERY SYSTEM, a class II device, cleared for Medical Device Technologies, Inc. on under FDA product code FDX (Endoscopic Cytology Brush). FDA's definition for product code FDX reads: "To collect cells for cytological evaluation". FDA records list 46 510(k) clearances for Medical Device Technologies, Inc., from to . As of , FDA records show no recalls naming K960004.

Clearance record

Decision date
Received
(78 days to decision)
Product code
FDX Endoscopic Cytology Brush
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Medical Device Technologies, Inc. 9191 Towne Centre Dr., #420, San Diego CA
510(k) summary
Summary
Third party review
No

Clearances, product code FDX

Trailing 12 months
1 clearance under product code FDX in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FDX, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260