Netech Corp

FDA Filings

This page includes the latest FDA filings for Netech Corp. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number2436826
FEI Number1000522032
NameNETECH CORP.
Owner & OperatorNETECH CORPORATION
Contact Address110 TOLEDO ST. --
Farmingdale NY 11735 US
Official Correspondent
  • MOHAN - DAS
  • x-631-5310100-11
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address110 TOLEDO ST.
FARMINGDALE, NY 11735 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
NETECH CORPORATION
External Pacemaker Analyzer 9602023-07-11
NETECH CORPORATION
Defibrillator / Transcutaneous Pacemaker Analyzer 6602020-03-13
Netech Corporation
Delta 33002019-08-28
NETECH CORPORATION
External Pacemaker Ananlyzer 9502018-07-20
NETECH CORPORATION
Defibrillator Analyzer 6502018-07-20
NETECH CORP. [NETECH CORPORATION]
MiniSim 10002014-07-03
NETECH CORP. [NETECH CORPORATION]
DigiFlow 10002014-07-03
NETECH CORP. [NETECH CORPORATION]
Delta 30002012-04-09
NETECH CORP. [NETECH CORPORATION]
Delta 22002012-04-09
NETECH CORP. [NETECH CORPORATION]
Delta 16002012-04-09
NETECH CORP. [NETECH CORPORATION]
Delta 15002012-04-09
NETECH CORP. [NETECH CORPORATION]
EXPMT 20002012-04-09
NETECH CORP.
DEFIBRILLATOR ANALYZER, DELTA 10001996-10-29
NETECH CORP. [NETECH CORPORATION]
MiniSim EEG1996-02-29
NETECH CORP. [NETECH CORPORATION]
DigiMano 25001995-10-11
NETECH CORP. [NETECH CORPORATION]
DigiMano 20001995-10-11
NETECH CORP. [NETECH CORPORATION]
DigiMano 10001995-10-11
NETECH CORP. [NETECH CORPORATION]
MutiPro 20001995-09-15
NETECH CORP. [NETECH CORPORATION]
LKG 6101995-09-15
NETECH CORP. [NETECH CORPORATION]
LKG 6011995-09-15

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