510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
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K123194Substantially Equivalent

Junctional Emergency Treatment Tool Model 30-0088

North American Rescue Products, Inc., Greer SC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K123194 is the FDA 510(k) clearance record for JUNCTIONAL EMERGENCY TREATMENT TOOL MODEL 30-0088, a class II device, cleared for North American Rescue Products, Inc. on under FDA product code DXC (Clamp, Vascular). FDA records list one 510(k) clearance for North American Rescue Products, Inc. As of , FDA records show one recall naming K123194.

Clearance record

Decision date
Received
(84 days to decision)
Product code
DXC Clamp, Vascular
Regulation
21 CFR 870.4450
Device class
Class II
Review panel
Cardiovascular
Applicant
North American Rescue Products, Inc. 35 Tedwall Ct., Greer SC
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DXC

Trailing 12 months
6 clearances under product code DXC in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DXC, trailing twelve months
MonthClearances
November 20251
December 20251
January 20260
February 20260
March 20260
April 20261
May 20261
June 20261
July 20261
August 20260
September 20260
October 20260