LIFE PLASMA

FDA Device Registration & Listing · Reading, PA, US · Registration 3021916912

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3021916912
FEI Number
3021916912
Entity Name
LIFE PLASMA
City/State/Country
Reading, PA, US
Establishment Address
5438 Perkiomen Ave, Reading, PA 19606, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Life Plasma (Owner Number: 10087532)
Owner / Operator Contact Address
5438 Perkiomen Ave, Reading, PA 19606, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
BK230814
PMA Number
N/A

All Registered Proprietary Names

SMARTDMS

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MMH Blood Establishment Computer Software And Accessories Hematology Class 2 864.9165 2024-09-25

Official Correspondent

Nagesh Ramesh

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Life Plasma
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3021916912. Last updated year: 2026. Please use registration number 3021916912 when referencing this establishment in official correspondence.
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