HAND-HELD NEBULIZER
K-Number: K940257 · 1994-10-13
Advertisement
Device Summary
Frequently Asked Questions
What is the HAND-HELD NEBULIZER?
HAND-HELD NEBULIZER is a medical device that received FDA 510(k) clearance on 1994-10-13. The listed applicant is Nutec, Inc.. The 510(k) number is K940257.
When did HAND-HELD NEBULIZER receive FDA 510(k) clearance?
HAND-HELD NEBULIZER received FDA 510(k) clearance on 1994-10-13, under 510(k) number K940257.
Who is the listed applicant for HAND-HELD NEBULIZER?
The FDA 510(k) record lists Nutec, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HAND-HELD NEBULIZER?
The FDA product code for HAND-HELD 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 Nutec, 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.
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