ALERKAN LTD

FDA Device Registration & Listing · Saray-Kazan Ankara, TR · Registration 3009509998

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
3009509998
FEI Number
3009509998
Entity Name
ALERKAN LTD
City/State/Country
Saray-Kazan Ankara, TR
Establishment Address
Keresteciler Sanayi Sitesi, A. Menderes Bulvari No: 3, Saray-Kazan Ankara 06980, TR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
ALERKAN Ltd (Owner Number: 10039179)
Owner / Operator Contact Address
Keresteciler Sanayi Sitesi, A. Menderes Bulvari No: 3, Saray-Kazan, TR-06 06980, TR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K111587
PMA Number
N/A

All Registered Proprietary Names

Alerkan Spirometry Filters, various sizes

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BZG Spirometer, Diagnostic Anesthesiology Class 2 868.1840 2011-12-14

Official Correspondent

No official correspondent registered.

US Agent Details

Sebastian Feye Business: Accurate Consultants Inc Email: sebastian@accuratefdaconsulting.com Phone: (619) 5170673

Related Public Records

Same Entity

ALERKAN Ltd
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
K923989 Sensor Medics Corp. SENSORMEDICS MODEL 6200 AUTOBOX DL 1993-08-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009509998. Last updated year: 2026. Please use registration number 3009509998 when referencing this establishment in official correspondence.
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