VIRCHOW MEDICAL, INC.

FDA Device Registration & Listing · San Diego, CA, US · Registration 3036035172

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
3036035172
FEI Number
3036035172
Entity Name
VIRCHOW MEDICAL, INC.
City/State/Country
San Diego, CA, US
Establishment Address
9191 Towne Centre Dr Ste 150, San Diego, CA 92122, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Virchow Medical, Inc. (Owner Number: 10092858)
Owner / Operator Contact Address
9191 Towne Centre Drive, Suite 150, San Diego, CA 92122, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

The Crow's Nest Biopsy Catchment System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NNK Container, Specimen Mailer And Storage, Non-Sterile Pathology Class 1 864.3250 2025-02-27

Official Correspondent

Alexander Arrow

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Virchow Medical, Inc.
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 3036035172. Last updated year: 2026. Please use registration number 3036035172 when referencing this establishment in official correspondence.
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