NETECH CORP.

FDA Device Registration & Listing · E Farmingdale, NY, US · Registration 2436826

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
2436826
FEI Number
1000522032
Entity Name
NETECH CORP.
City/State/Country
E Farmingdale, NY, US
Establishment Address
110 TOLEDO ST., E Farmingdale, NY 11735, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
NETECH CORPORATION (Owner Number: 9021637)
Owner / Operator Contact Address
110 TOLEDO ST., --, Farmingdale, NY 11735, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Digimano 2000 Digimano 2500 Digimano 1000 Digiflow 2000 LKG 601 LKG 610 Multipro 2000 EXPMT 2000 Minisim 1000 Advanced Minisim 1000 Basic Delta 1600 Delta 3300

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JYJ Gauge, Measuring Ear, Nose, Throat Class 1 874.4420 1995-10-11
BXY Flowmeter, Calibration, Gas Anesthesiology Class 1 868.2350 2014-07-03
DSM Alarm, Leakage Current, Portable Cardiovascular Class 1 870.2640 1995-09-15
DTC Analyzer, Pacemaker Generator Function Cardiovascular Class 2 870.3630 2012-04-09
GYA Tester, Electrode/Lead, Electroencephalograph Neurology Class 1 882.1410 2014-07-03
DRL Tester, Defibrillator Cardiovascular Class 2 870.5325 2012-04-09

Official Correspondent

MOHAN DAS

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

NETECH CORPORATION
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
K882327 Oscor Medical Corp. PACER SENSING ANALYZER (PSA 100) 1988-10-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2436826. Last updated year: 2026. Please use registration number 2436826 when referencing this establishment in official correspondence.
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