MICRO-MIST NEBULIZER
K-Number: K904196 · 1990-12-21
Advertisement
Device Summary
Frequently Asked Questions
What is the MICRO-MIST NEBULIZER?
MICRO-MIST NEBULIZER is a medical device that received FDA 510(k) clearance on 1990-12-21. The listed applicant is Bp , Ltd.. The 510(k) number is K904196.
When did MICRO-MIST NEBULIZER receive FDA 510(k) clearance?
MICRO-MIST NEBULIZER received FDA 510(k) clearance on 1990-12-21, under 510(k) number K904196.
Who is the listed applicant for MICRO-MIST NEBULIZER?
The FDA 510(k) record lists Bp , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICRO-MIST NEBULIZER?
The FDA product code for MICRO-MIST NEBULIZER is CAF.
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.
Other records listing Bp , Ltd. 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.
Related Devices (Code: CAF)
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.
Advertisement