EKOM SPOL. S R.O.

FDA Device Registration & Listing · PIESTANY Trnavsky, SK · Registration 3005245901

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
3005245901
FEI Number
3005245901
Entity Name
EKOM SPOL. S R.O.
City/State/Country
PIESTANY Trnavsky, SK
Establishment Address
PRIEMYSELNA 5031/18, PIESTANY Trnavsky 921 01, SK
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
EKOM SPOL. S R.O. (Owner Number: 9074921)
Owner / Operator Contact Address
PRIEMYSELNA 5031/18, --, PIESTANY, SK-NOTA 921 01, SK
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

DK50 DS C235 Air 550 compressor

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BTI Compressor, Air, Portable Anesthesiology Class 2 868.6250 2009-11-19
BTI Compressor, Air, Portable Anesthesiology Class 2 868.6250 2015-01-07

Official Correspondent

JULIUS IVAN

US Agent Details

Matt Dryden Business: Promedic, Inc. Email: matt.dryden@promedic.cc Phone: (239) 3076060

Related Public Records

Same Entity

EKOM SPOL. S R.O.
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
K900686 Medical Industries America, Inc. MAXI COMPRESSORS 1990-04-26

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005245901. Last updated year: 2026. Please use registration number 3005245901 when referencing this establishment in official correspondence.
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