510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K202073Substantially Equivalent

NeedleSmart Professional (NS Pro)

Needlesmart Limited, Knowsley, Prescot, GB / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K202073 is the FDA 510(k) clearance record for NeedleSmart Professional (NS Pro), a class II device, cleared for Needlesmart Limited on under FDA product code MTV (Sharps Needle Destruction Device). FDA's definition for product code MTV reads: "A prescription device that is intended to destroy needles or sharps used for medical purposes by incineration or mechanical means". FDA records list one 510(k) clearance for Needlesmart Limited. As of , FDA records show no recalls naming K202073.

Clearance record

Decision date
Received
(241 days to decision)
Product code
MTV Sharps Needle Destruction Device
Regulation
21 CFR 880.6210
Device class
Class II
Review panel
General Hospital
Applicant
Needlesmart Limited Suite 2b, Stanley Grange Business Park, Ormskirk Rd., Knowsley, Prescot, GB
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MTV

Trailing 12 months

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

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