PCCI, INC

FDA Device Registration & Listing · ALEXANDRIA, VA, US · Registration 3004035771

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
3004035771
FEI Number
3004035771
Entity Name
PCCI, INC
City/State/Country
ALEXANDRIA, VA, US
Establishment Address
300 N LEE ST STE 201, ALEXANDRIA, VA 22314, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
PCCI, INC (Owner Number: 9104700)
Owner / Operator Contact Address
300 N LEE STREET, Suite 201, Alexandria, VA 22314, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K102831
PMA Number
N/A

All Registered Proprietary Names

PCCI Lifeforce Clinical Hyperbaric Facility T Class Hyperbaric Facilities Ods1 - Hood Driver Althea 4200

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CBF Chamber, Hyperbaric Anesthesiology Class 2 868.5470 2022-08-10
CBF Chamber, Hyperbaric Anesthesiology Class 2 868.5470 2016-11-09
CBF Chamber, Hyperbaric Anesthesiology Class 2 868.5470 2016-11-09
CBF Chamber, Hyperbaric Anesthesiology Class 2 868.5470 2022-08-10

Official Correspondent

Jenny Miller

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PCCI, INC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004035771. Last updated year: 2026. Please use registration number 3004035771 when referencing this establishment in official correspondence.
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