SYNTEVENT ATOMIZER/NEBULIZER AEROSOL
K-Number: K822625 · 1982-10-13
Advertisement
Device Summary
Frequently Asked Questions
What is the SYNTEVENT ATOMIZER/NEBULIZER AEROSOL?
SYNTEVENT ATOMIZER/NEBULIZER AEROSOL is a medical device that received FDA 510(k) clearance on 1982-10-13. The listed applicant is Syva Co.. The 510(k) number is K822625.
When did SYNTEVENT ATOMIZER/NEBULIZER AEROSOL receive FDA 510(k) clearance?
SYNTEVENT ATOMIZER/NEBULIZER AEROSOL received FDA 510(k) clearance on 1982-10-13, under 510(k) number K822625.
Who is the listed applicant for SYNTEVENT ATOMIZER/NEBULIZER AEROSOL?
The FDA 510(k) record lists Syva Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYNTEVENT ATOMIZER/NEBULIZER AEROSOL?
The FDA product code for SYNTEVENT ATOMIZER/NEBULIZER AEROSOL 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.
Other records listing Syva Co. 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: 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.
Advertisement