Cleared Traditional

K142469 - 2D Mercy TAPE & 3D Mercy TAPE (FDA 510(k) Clearance)

May 2015
Decision
240d
Days
Class 1
Risk

K142469 is an FDA 510(k) clearance for the 2D Mercy TAPE & 3D Mercy TAPE. This device is classified as a Mercy Tape 2d And 3d Models (Class I - General Controls, product code PIR).

Submitted by Children'S Mercy Hospital (Kansas City, US). The FDA issued a Cleared decision on May 1, 2015, 240 days after receiving the submission on September 3, 2014.

This device falls under the General Hospital FDA review panel. Regulated under 21 CFR 878.4800. The Mercy Tape Device (2d And 3d Models) Is Intended For Use By Health Care Professionals To Estimate The Body Weight Of Pediatric Patients Between The Ages Of 2 Months And 16 Years, Using Linear Measurements From Specific Anatomical Landmarks Made With The Tape Device For Humeral Length (hl, For The 2d Model) Or Half-humeral Length (hhl, For The 3d Model) And The Mid-upper Arm Circumference (muac)..

Submission Details

510(k) Number K142469 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 03, 2014
Decision Date May 01, 2015
Days to Decision 240 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF

Device Classification

Product Code PIR - Mercy Tape 2d And 3d Models
Device Class Class I - General Controls
CFR Regulation 21 CFR 878.4800
Definition The Mercy Tape Device (2d And 3d Models) Is Intended For Use By Health Care Professionals To Estimate The Body Weight Of Pediatric Patients Between The Ages Of 2 Months And 16 Years, Using Linear Measurements From Specific Anatomical Landmarks Made With The Tape Device For Humeral Length (hl, For The 2d Model) Or Half-humeral Length (hhl, For The 3d Model) And The Mid-upper Arm Circumference (muac).