LUNDY VAPORIZER SYSTEM
K-Number: K884090 · 1989-01-24
Advertisement
Device Summary
Frequently Asked Questions
What is the LUNDY VAPORIZER SYSTEM?
LUNDY VAPORIZER SYSTEM is a medical device that received FDA 510(k) clearance on 1989-01-24. The listed applicant is Vaporflow Technology, Inc.. The 510(k) number is K884090.
When did LUNDY VAPORIZER SYSTEM receive FDA 510(k) clearance?
LUNDY VAPORIZER SYSTEM received FDA 510(k) clearance on 1989-01-24, under 510(k) number K884090.
Who is the listed applicant for LUNDY VAPORIZER SYSTEM?
The FDA 510(k) record lists Vaporflow Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LUNDY VAPORIZER SYSTEM?
The FDA product code for LUNDY VAPORIZER SYSTEM is CAD.
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: CAD)
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