Em-Scan HP-2 Pediatric Body Composition Analyzer

FDA 510(k) K902042 · Em-Scan, Inc.

Substantially Equivalent

510(k) numberK902042

Submission

Device name
Em-Scan HP-2 Pediatric Body Composition Analyzer
Applicant
Em-Scan, Inc.
Washington, DC, US
Received
May 4, 1990
Decision date
July 26, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DSB – Plethysmograph, Impedance
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2770
Specialty
Cardiovascular

Other 510(k)s with product code DSB

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K243727Re:BalansDSB · Traditional Mode Sensors AS10/16/2025SE
K250922Edema Guard Monitor (EGM) CardioSet-001DSB · Traditional Cardioset Medical , Ltd.09/09/2025SE
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K223217Zynex Monitoring System, Model CM-1600DSB · Traditional Zynex Medical, Inc.06/16/2023SE
K211585Bodyport Cardiac ScaleDSB · Traditional Bodyport, Inc.07/29/2022SE
K203473SozoDSB · Traditional ImpediMed Limited04/19/2021SE
K193410SOZO Body Fluid AnalyzerDSB · Traditional ImpediMed Limited10/02/2020SE
K191697Cardiac Monitor 1500DSB · Traditional Zynex Medical, Inc.02/21/2020SE

Questions and answers

When was Em-Scan HP-2 Pediatric Body Composition Analyzer cleared by the FDA?

Em-Scan HP-2 Pediatric Body Composition Analyzer (K902042) received a 510(k) decision of Substantially Equivalent on July 26, 1990, 83 days after the submission was received.

What is the product code of K902042?

The FDA product code is DSB – Plethysmograph, Impedance, a Class II (moderate risk) device regulated under 21 CFR 870.2770.