SILVER LAKE RESEARCH CORPORATION

FDA Device Registration & Listing · Azusa, CA, US · Registration 3014308364

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
3014308364
FEI Number
3014308364
Entity Name
SILVER LAKE RESEARCH CORPORATION
City/State/Country
Azusa, CA, US
Establishment Address
1300 West Optical Drive, Suite 300, Azusa, CA 91702, US
Establishment Type(s)
Manufacture Device in the United States for Export Only
Owner / Operator
Silver Lake Research Corporation (Owner Number: 10056750)
Owner / Operator Contact Address
1300 West Optical Drive, Suite 300, Azusa, CA 91702, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

HemoTypeSC

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PDC Investigational Use Only - Hematology Unknown Class N N/A 2021-01-11

Official Correspondent

SLRC INFO

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Silver Lake Research Corporation
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 3014308364. Last updated year: 2026. Please use registration number 3014308364 when referencing this establishment in official correspondence.
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