510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K240295Substantially Equivalent

InstaStrip Fentanyl Rapid Test (Urine); InstaStrip Fentanyl Dipstick Test (Urine)

Instanosis Inc., King Of Prussia PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K240295 is the FDA 510(k) clearance record for InstaStrip Fentanyl Rapid Test (Urine); InstaStrip Fentanyl Dipstick Test (Urine), a class II device, cleared for Instanosis, Inc. on under FDA product code NGL (Test, Opiates, Over The Counter). FDA records list one 510(k) clearance for Instanosis, Inc. As of , FDA records show no recalls naming K240295.

Clearance record

Decision date
Received
(56 days to decision)
Product code
NGL Test, Opiates, Over The Counter
Regulation
21 CFR 862.3650
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Instanosis, Inc. 1004 W 9th Ave., King Of Prussia PA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NGL

Trailing 12 months
1 clearance under product code NGL 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 NGL, 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