Comar

FDA Device Registration & Listing · Rancho Cucamonga, CA, US · Registration 3004601221

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
3004601221
FEI Number
3004601221
Entity Name
Comar
City/State/Country
Rancho Cucamonga, CA, US
Establishment Address
9595 Utica Ave, Rancho Cucamonga, CA 91730, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Comar LLC / PCI (Owner Number: 9084326)
Owner / Operator Contact Address
220 Laurel Rd., STE. 201, Voorhees, NJ 08043, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Rika Plasma Bottle

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GKT Separator, Automated, Blood Cell, Diagnostic Hematology Class 2 864.9245 2022-09-02

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Comar LLC / PCI
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 3004601221. Last updated year: 2026. Please use registration number 3004601221 when referencing this establishment in official correspondence.
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