SOLOMON PARK RESEARCH LABORATORIES, INC.

FDA Device Registration & Listing · Burien, WA, US · Registration 3023437

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
3023437
FEI Number
3023437
Entity Name
SOLOMON PARK RESEARCH LABORATORIES, INC.
City/State/Country
Burien, WA, US
Establishment Address
658 S 152nd St, Burien, WA 98148, US
Establishment Type(s)
Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Solomon Park Research Laboratories, Inc. (Owner Number: 10092524)
Owner / Operator Contact Address
658 S. 152ND St., Burien, WA 98148, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Vitamin D Controls Lipoprotein Controls LRC Electrolyte Panel

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JIX Calibrator, Multi-Analyte Mixture Clinical Chemistry Class 2 862.1150 2025-01-16

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Solomon Park Research Laboratories, 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
K041905 Instrumentation Laboratory CO HEMOSIL CALIBRATION PLASMA 2004-09-28
K081103 Siemens Healthcare Diagnostics, Inc. LOCI THYROID CALIBRATOR WITH MODEL RC610 2008-05-23

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0164-2015 Siemens Healthcare Diagnostics, Inc 2
Siemens Calibrator E; SMN 10309079 (2 pack), SMN 10321075 (6 pack), SMN 10335532 (6 pack Ref)

Similar Registrations

Registration Number Establishment Name Location
3005333358 ABBOTT LABORATORIES Lake Forest, IL, US
3002642396 Ortho Clinical Diagnostics Singapore South West, SG
9610126 ROCHE DIAGNOSTICS GMBH MANNHEIM Baden-Wurttemberg, DE
2050010 BECKMAN COULTER, INC. CARLSBAD, CA, US
3003593973 Infrared Laboratory Systems dba SYNERMED WESTFIELD, IN, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3023437. Last updated year: 2026. Please use registration number 3023437 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.