Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3002303857

FEI Number

3002303857

Entity Name

ACTIONPAK, INC.

City/State/Country

Camden, NJ, US

Establishment Address

1600 River Avenue, Camden, NJ 08105, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

ActionPak, Inc. (Owner Number: 10043895)

Owner / Operator Contact Address

1600 River Avenue, Camden, NJ 08105, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Pulse Oximeter

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OCH	Oximeter, Infrared, Sporting, Aviation	Cardiovascular	Class 2	870.2700	2013-04-03

Official Correspondent

Ira Smith

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ActionPak, Inc.

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 3002303857. Last updated year: 2026. Please use registration number 3002303857 when referencing this establishment in official correspondence.