APPLIED PHOTONIX LLC

FDA Device Registration & Listing · Tampa, FL, US · Registration 3032191707

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
3032191707
FEI Number
3032191707
Entity Name
APPLIED PHOTONIX LLC
City/State/Country
Tampa, FL, US
Establishment Address
3802 Spectrum Blvd suite 202, Tampa, FL 33612, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Applied Photonix LLC (Owner Number: 10091316)
Owner / Operator Contact Address
3802 Spectrum Blvd suite 202, Tampa, FL 33612, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K241140
PMA Number
N/A

All Registered Proprietary Names

ViroZap

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FRA Purifier, Air, Ultraviolet, Medical General Hospital Class 2 880.6500 2024-08-21

Official Correspondent

Lovely Goswami

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Applied Photonix LLC
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 3032191707. Last updated year: 2026. Please use registration number 3032191707 when referencing this establishment in official correspondence.
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