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
K874665Unknown

Securline Fine Needle Aspiration Biopsy Tray

Precision Dynamics Corporation, Van Nuys CA / Traditional, Unknown
FDA source (opens on fda.gov)

K874665 is the FDA 510(k) clearance record for SECURLINE FINE NEEDLE ASPIRATION BIOPSY TRAY, a class I device, cleared for Precision Dynamics Corp. on under FDA product code LRP (Tray, Surgical). FDA records list 26 510(k) clearances for Precision Dynamics Corp., from to . As of , FDA records show no recalls naming K874665.

Clearance record

Decision date
Received
(68 days to decision)
Product code
LRP Tray, Surgical
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Precision Dynamics Corp. Post Office Box 9043, Van Nuys CA
Third party review
No

Clearances, product code LRP

Trailing 12 months

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

FDA records show no clearances under product code LRP in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LRP, 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