COMPUTATIONAL DIAGNOSTICS, INC.

FDA Device Registration & Listing · Oakland, PA, US · Registration 2530126

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
2530126
FEI Number
1000221291
Entity Name
COMPUTATIONAL DIAGNOSTICS, INC.
City/State/Country
Oakland, PA, US
Establishment Address
5001 Baum Blvd Ste 530, Oakland, PA 15213, US
Establishment Type(s)
Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
COMPUTATIONAL DIAGNOSTICS, INC. (Owner Number: 9001018)
Owner / Operator Contact Address
5001 BAUM BLVD., Suite 530, Pittsburgh, PA 15213, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

NN650 NN690 NN600 NeuroNet NNRMS NN680

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GWF Stimulator, Electrical, Evoked Response Neurology Class 2 882.1870 2009-02-10

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

COMPUTATIONAL DIAGNOSTICS, INC.
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
K880088 Cadwell Laboratories, Inc. CADWELL EXCEL 1988-05-04

Similar Registrations

Registration Number Establishment Name Location
3018708317 MAGNUS MEDICAL INC. Burlingame, CA, US
1221763 ARCH Medical Solutions - Seabrook SEABROOK, NH, US
3008773490 PAUL E. DANCHELL A/S Jyderup Sjalland, DK
9611252 NIHON KOHDEN CORP. SHINJUKU-KU Tokyo, JP
3009959868 Ferry Machine Corporation Little Ferry, NJ, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2530126. Last updated year: 2026. Please use registration number 2530126 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.