Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

KOKOMATE

K-Number: K022276 · 2002-10-04

ApplicantFerraris Respiratory, Inc.
Decision Date2002-10-04
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

KOKOMATE is the device name listed in this FDA 510(k) record. The listed applicant is Ferraris Respiratory, Inc.. It received FDA 510(k) clearance on 2002-10-04 under 510(k) number K022276. The device is classified under product code BZG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KOKOMATE?

KOKOMATE is a medical device that received FDA 510(k) clearance on 2002-10-04. The listed applicant is Ferraris Respiratory, Inc.. The 510(k) number is K022276.

When did KOKOMATE receive FDA 510(k) clearance?

KOKOMATE received FDA 510(k) clearance on 2002-10-04, under 510(k) number K022276.

Who is the listed applicant for KOKOMATE?

The FDA 510(k) record lists Ferraris Respiratory, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KOKOMATE?

The FDA product code for KOKOMATE is BZG.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Ferraris Respiratory, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K914272KOKO SPIROMETER

Related Devices (Code: BZG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K251777MESI mTABLET SPIROMesi D.O.O.K241843TD-7301 Spirometer (TD-7301)Gostar Co., Ltd.K231416Air Next (NVD-02)Nuvoair ABK230501Spirobank OxiMir Medical International Research USAK230178EasyOne Sky SpirometerNdd Medizintechnik AGK222525Alveoair Digital SpirometerRoundworks Technologies Private Limited

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑