Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K993850Substantially Equivalent

Urinalysis Reagent Strips (10 Parameters)

International Newtech Development, Inc., Delta, B.C., CA / Traditional, Substantially Equivalent

K993850 is the FDA 510(k) clearance record for URINALYSIS REAGENT STRIPS (10 PARAMETERS), a class I device, cleared for International Newtech Development, Inc. on under FDA product code JMT (Diazo (Colorimetric), Nitrite (Urinary, Non-Quant)). FDA records list 8 510(k) clearances for International Newtech Development, Inc., from to . As of , FDA records show 2 recalls naming K993850.

Clearance record

Decision date
Received
(52 days to decision)
Product code
JMT Diazo (Colorimetric), Nitrite (Urinary, Non-Quant)
Regulation
21 CFR 862.1510
Device class
Class I
Review panel
Clinical Chemistry
Applicant
International Newtech Development, Inc. 1629 Fosters Way, Delta, B.C., CA
510(k) summary
Statement
Third party review
No

Clearances, product code JMT

Trailing 12 months
1 clearance under product code JMT 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 JMT, 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