Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3038259592

FEI Number

3038259592

Entity Name

ZOLL MEDICAL CORPORATION

City/State/Country

Wilmington, MA, US

Establishment Address

38 Upton Dr, Wilmington, MA 01887, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

ZOLL Medical Corporation (Owner Number: 1220908)

Owner / Operator Contact Address

269 MILL ROAD, Chelmsford, MA 01824, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

P160022

All Registered Proprietary Names

ACCUVENT SENSOR DISPOSABLE FLOWTUBE, ACCUVENT FLOW SENSOR CONNECTOR, ACCUVENT Eagle II AEV EMV+

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BXP	Transducer, Gas Flow	Anesthesiology	Class 1	868.2885	2026-05-12
CBK	Ventilator, Continuous, Facility Use	Anesthesiology	Class 2	868.5895	2017-09-18
DQA	Oximeter	Cardiovascular	Class 2	870.2700	2017-09-18
BTA	Pump, Portable, Aspiration (Manual Or Powered)	General, Plastic Surgery	Class 2	878.4780	2017-05-17
MKJ	Automated External Defibrillators (Non-Wearable)	Cardiovascular	Class 3	870.5310	2017-05-31
MKJ	Automated External Defibrillators (Non-Wearable)	Cardiovascular	Class 3	870.5310	2018-01-18

Official Correspondent

Paul Dias

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ZOLL Medical Corporation

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
1218058	ZOLL Medical Corporation	Pawtucket, RI, US
2112020	ZOLL Medical Corporation	DEERFIELD, WI, US
2021710	ZOLL Palm Springs	Palm Springs, CA, US
3029871637	ZOLL International Holding B.V.	Elst Gelderland, NL
3010617000	ZOLL Circulation, Inc.	San Jose, CA, US

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K051895	Datex-Ohmeda, Inc.	GE DATEX-OHMEDA ENGSTROM CARESTATION	2005-09-27
K082966	Covidien, Formerly Nellcor Puritan Bennett, Inc.	PB 540 VENTILATOR	2008-10-31
K903523	Hewlett-Packard Co.	HP MODEL M1020A, ARTERIAL OXYGEN SAT/PLETH MODULE	1990-10-23
K973147	Nellcor Puritan Bennett, Inc.	NPB-295 PULSE OXIMETER	1997-11-14
K231243	Guangdong Genial Technology Co., Ltd.	Finger Clip Pulse Oximeter	2023-10-31

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0008-2015	Respironics California Inc	2	Esprit V1000 and V200 Ventilators, Model No. V1000 and V200; and the 3rd Generation Power Supply Repair Part (RP)Kits Microprocessor-controlled, electrically powered mechanical ventilators intended for use by qualified medical personnel to provide continuous or intermittent ventilator support for adult, pediatric and neonatal patients as prescribed by a physician.
Z-0018-2011	Draeger Medical Systems, Inc.	2	Oxylog 3000, Emergency and Transport Ventilator; Catalog #2M86300; Drager Medical Inc., 3135 Quarry Road, Telford, PA 18969.
Z-0112-2015	Nellcor Puritan Bennett Inc. (dba Covidien LP)	2	Covidien Puritan Bennett 980 Ventilator, Rx ONLY. Suitable for service in a hospital (institutions) and intra-hospital transport to provide continuous positive pressure ventilator for Neonatal (NICU) through Adult patient populations.
Z-0180-2015	Nellcor Puritan Bennett Inc. (dba Covidien LP)	2	Covidien Puritan Bennett 980 Ventilator, Rx ONLY, Made in Ireland., Covidien LLC, USA. REF 980X1ENDIUU.
Z-0338-2022	Covidien Llc	2	Puritan Bennett 980 Series Ventilator, 980A1ENNISB

Similar Registrations

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2183890	UNIPOWER CORP.	Minnetonka, MN, US
3038562397	Respironics Medical Products (Shenzhen) Co., Ltd.	Shenzhen Guangdong, CN
9614485	NDD MEDIZINTECHNIK AG	ZURICH, CH
9710567	Besmed Health Business Corporation	New Taipei City, TW
3012309966	ENGLERT GMBH & CO. KG	Wertheim Baden-Wurttemberg, DE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3038259592. Last updated year: 2026. Please use registration number 3038259592 when referencing this establishment in official correspondence.