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)

NEBULIZER CHRONOLOG & INTERPRETER

K-Number: K823423 · 1982-12-15

Decision Date1982-12-15
Product CodeCCQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NEBULIZER CHRONOLOG & INTERPRETER is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Technology Products, Inc.. It received FDA 510(k) clearance on 1982-12-15 under 510(k) number K823423. The device is classified under product code CCQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEBULIZER CHRONOLOG & INTERPRETER?

NEBULIZER CHRONOLOG & INTERPRETER is a medical device that received FDA 510(k) clearance on 1982-12-15. The listed applicant is Advanced Technology Products, Inc.. The 510(k) number is K823423.

When did NEBULIZER CHRONOLOG & INTERPRETER receive FDA 510(k) clearance?

NEBULIZER CHRONOLOG & INTERPRETER received FDA 510(k) clearance on 1982-12-15, under 510(k) number K823423.

Who is the listed applicant for NEBULIZER CHRONOLOG & INTERPRETER?

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

What is the FDA product code for NEBULIZER CHRONOLOG & INTERPRETER?

The FDA product code for NEBULIZER CHRONOLOG & INTERPRETER is CCQ.

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.

Related Devices (Code: CCQ)

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.

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.

↑