CISION VISION

FDA Device Registration & Listing · Mountain View, CA, US · Registration 3021382079

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
3021382079
FEI Number
3021382079
Entity Name
CISION VISION
City/State/Country
Mountain View, CA, US
Establishment Address
319 N Bernardo Avenue,, ATTN: Cision Vision, Mountain View, CA 94043, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
Cision Vision (Owner Number: 10084025)
Owner / Operator Contact Address
319 N Bernardo Avenue,, ATTN: Cision Vision, Mountain View, CA 94043, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Cision InVision

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IBM Microscope, Phase Contrast Pathology Class 1 864.3600 2022-01-10

Official Correspondent

Zhongming Li

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Cision Vision
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 3021382079. Last updated year: 2026. Please use registration number 3021382079 when referencing this establishment in official correspondence.
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