PEDIA

FDA Device Registration & Listing · Fairfax, VA, US · Registration 3014729687

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
3014729687
FEI Number
3014729687
Entity Name
PEDIA
City/State/Country
Fairfax, VA, US
Establishment Address
2804 Albany Court, Fairfax, VA 22031, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
PeDIA (Owner Number: 10061544)
Owner / Operator Contact Address
2804 Albany Court, Fairfax, VA 22031, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K181424
PMA Number
N/A

All Registered Proprietary Names

PeDIA

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BTC Bag, Reservoir Anesthesiology Class 1 868.5320 2019-10-28

Official Correspondent

Diane Miller

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PeDIA
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 3014729687. Last updated year: 2026. Please use registration number 3014729687 when referencing this establishment in official correspondence.
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