CARROT MEDICAL, LLC

FDA Device Registration & Listing · Bothell, WA, US · Registration 3007540658

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
3007540658
FEI Number
3007540658
Entity Name
CARROT MEDICAL, LLC
City/State/Country
Bothell, WA, US
Establishment Address
22122 20TH AVE SE STE H-166, Bothell, WA 98021, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
Carrot Medical, LLC (Owner Number: 10028543)
Owner / Operator Contact Address
22122 20th Avenue SE, Suite H-166, Bothell, WA 98021, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K083321
PMA Number
N/A

All Registered Proprietary Names

CardioView C-View

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DXJ Display, Cathode-Ray Tube, Medical Cardiovascular Class 2 870.2450 2009-02-10

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Carrot Medical, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K180534 Philips Medizin Systeme Boeblingen GmbH Philips IntelliVue GuardianSoftware 2018-07-16
K161767 Philips Medizin Systeme Boeblingen GmbH Philips IntelliVue GuardianSoftware 2017-01-27
K212208 Philips Medizin Systeme Boeblingen GmbH Philips IntelliVue GuardianSoftware (Rev. E.0X) 2021-09-30

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9610816 Philips Medizin Systeme Boeblingen GmbH BOEBLINGEN Baden-Wurttemberg, DE
3029871637 ZOLL International Holding B.V. Elst Gelderland, NL
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007540658. Last updated year: 2026. Please use registration number 3007540658 when referencing this establishment in official correspondence.
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