INTERCARE DX, INC.

FDA Device Registration & Listing · TORRANCE, CA, US · Registration 3005735282

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
3005735282
FEI Number
3005735282
Entity Name
INTERCARE DX, INC.
City/State/Country
TORRANCE, CA, US
Establishment Address
20280 S VERMONT AVE STE 215, TORRANCE, CA 90502, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
MERIDIAN HEALTH SYSTEMS, P.C. (Owner Number: 9084208)
Owner / Operator Contact Address
20280 South Vermont Avenue Suite#215, Torrance, CA 90502, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K011625
PMA Number
N/A

All Registered Proprietary Names

VASOCOR(TM) VASCULAR DIA InterCare Vascular Diagnostic Center

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DXN System, Measurement, Blood-Pressure, Non-Invasive Cardiovascular Class 2 870.1130 2006-03-13

Official Correspondent

ANTHONY DIKE, MD, FACP, FASPC

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MERIDIAN HEALTH SYSTEMS, P.C.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K100940 Andon Health Co, Ltd. FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR, MODEL KD-5965 2010-06-29
K251581 Shenzhen Hingmed Medical Instrument Co., Ltd. Wearable Ambulatory Blood Pressure Monitor (WBP-02A) 2026-02-13
K200521 Health & Life Co., Ltd. Full Automatic(NIBP) Blood Pressure Monitor 2020-06-12
K152003 Andon Health Co, Ltd. iHealth BP3L Wireless Blood Pressure Monitor 2015-09-24
K952827 Sein Electronics Co., Ltd. FULL AUTO WRIST BLOOD PRESSURE METER MODEL SE-5000 1996-11-14

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0032-2025 MEDLINE INDUSTRIES, LP Northfield 2
MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001
Z-0033-2025 MEDLINE INDUSTRIES, LP Northfield 2
MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001U.
Z-0034-2025 MEDLINE INDUSTRIES, LP Northfield 2
MEDLINE Automatic Digital Blood Pressure Monitor, REF MDS1001UT.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005735282. Last updated year: 2026. Please use registration number 3005735282 when referencing this establishment in official correspondence.
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