Pentair Filtration Solutions

FDA Device Registration & Listing · Saint Paul, MN, US · Registration 2132517

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
2132517
FEI Number
1000221012
Entity Name
Pentair Filtration Solutions
City/State/Country
Saint Paul, MN, US
Establishment Address
1350 Hammond Rd, Saint Paul, MN 55110, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Pentair Filtration Solutions (Owner Number: 9009435)
Owner / Operator Contact Address
1350 HAMMOND RD., --, Saint Paul, MN 55110, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K965020
PMA Number
N/A

All Registered Proprietary Names

DBF32, DBF24, DBF27,DBF25, DFC06, D DPB30 Disposable Pre-Bypass Filter DBF23 DISPOSABLE RESPIRATORY FILTER DPC20 Disposable Pre-Bypass Filter HUMIDIFLOW DBF23 Disposble Main Flow Filter DBF23 Reuseable Respiratory Filter

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CAH Filter, Bacterial, Breathing-Circuit Anesthesiology Class 2 868.5260 2007-12-20
KRJ Filter, Prebypass, Cardiopulmonary Bypass Cardiovascular Class 2 870.4280 2007-12-20
CAH Filter, Bacterial, Breathing-Circuit Anesthesiology Class 2 868.5260 2016-03-04
KRJ Filter, Prebypass, Cardiopulmonary Bypass Cardiovascular Class 2 870.4280 2007-12-20
BTT Humidifier, Respiratory Gas, (Direct Patient Interface) Anesthesiology Class 2 868.5450 2006-12-07
CAH Filter, Bacterial, Breathing-Circuit Anesthesiology Class 2 868.5260 2007-12-20
CAH Filter, Bacterial, Breathing-Circuit Anesthesiology Class 2 868.5260 2007-12-20

Official Correspondent

Roger Hanzalik

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Pentair Filtration Solutions
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
K962045 Mallinckrodt Medical ANESTHESIA BREATHING CIRCUIT/ANESTHESIA BREATHING KIT 1996-11-26
K012633 Respironics, Inc. RESPIRONICS HEATED HUMIDIFIER 2002-02-28
K970478 Marquest Medical Products, Inc. SCT 3000 HEATED HUMIDIFIER 1997-07-16

Similar Registrations

Registration Number Establishment Name Location
3007337939 FLODINS FILTER AB Lysekil Vastra Gotaland, SE
8021995 FLEXICARE MEDICAL LTD. RHONDDA CYNON TAFF Wales, GB
3007289408 Medline Canada Guelph Ontario, CA
9617604 ICU Medical Healthcare Manufacturing S.A. de C.V. Tijuana, B.C. C.P. Baja California, MX
3006783791 GaleMed (Xiamen) Co., Ltd. XIAMEN Fujian, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2132517. Last updated year: 2026. Please use registration number 2132517 when referencing this establishment in official correspondence.
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