BOEKEL SCIENTIFIC

FDA Device Registration & Listing · Feasterville, PA, US · Registration 3005953362

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
3005953362
FEI Number
3005953362
Entity Name
BOEKEL SCIENTIFIC
City/State/Country
Feasterville, PA, US
Establishment Address
855 Pennsylvania Blvd., Feasterville, PA 19053, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Boekel Scientific (Owner Number: 10030490)
Owner / Operator Contact Address
855 Pennsylvania Blvd., Feasterville, PA 19053, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
BK100051
PMA Number
N/A

All Registered Proprietary Names

301300 Boekel Large Platelet Agitator 301650 Boekel Large Platelet Incubator 301200 Boekel Small Platelet Agitator FS100 Boekel Floor Standing Platelet Incubator Agitator 301550 Boekel Small Platelet Incubator 145702 Boekel Tissue Bath III Standard 145951 Boekel Tissue Bath III Deluxe 14792 Boekel Tissue Bath 302000 Boekel Blood Collection Mixer 301000 Boekel Plasma Thawer

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KSH Chamber, Environmental For The Storage Of Platelet Concentrate Hematology Class 2 864.9575 2015-03-09
IDY Bath, Flotation, Tissue Pathology Class 1 864.3010 2009-10-08
KSQ Device, Blood Mixing And Blood Weighing Hematology Class 1 864.9195 2015-03-09
KZL Device, Warming. Blood And Plasma Hematology Class 2 864.9205 2011-05-26

Official Correspondent

Christopher Carsia

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Boekel Scientific
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005953362. Last updated year: 2026. Please use registration number 3005953362 when referencing this establishment in official correspondence.
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