PENLON PPV VAPORIZER
K-Number: K844007 · 1985-03-12
Advertisement
Device Summary
Frequently Asked Questions
What is the PENLON PPV VAPORIZER?
PENLON PPV VAPORIZER is a medical device that received FDA 510(k) clearance on 1985-03-12. The listed applicant is Penlon, Inc.. The 510(k) number is K844007.
When did PENLON PPV VAPORIZER receive FDA 510(k) clearance?
PENLON PPV VAPORIZER received FDA 510(k) clearance on 1985-03-12, under 510(k) number K844007.
Who is the listed applicant for PENLON PPV VAPORIZER?
The FDA 510(k) record lists Penlon, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PENLON PPV VAPORIZER?
The FDA product code for PENLON PPV VAPORIZER 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.
Other records listing Penlon, 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: 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