QUIK-FIL VAPORIZER KEYED FILLER
K-Number: K961468 · 1996-07-16
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Device Summary
Frequently Asked Questions
What is the QUIK-FIL VAPORIZER KEYED FILLER?
QUIK-FIL VAPORIZER KEYED FILLER is a medical device that received FDA 510(k) clearance on 1996-07-16. The listed applicant is Penlon , Ltd.. The 510(k) number is K961468.
When did QUIK-FIL VAPORIZER KEYED FILLER receive FDA 510(k) clearance?
QUIK-FIL VAPORIZER KEYED FILLER received FDA 510(k) clearance on 1996-07-16, under 510(k) number K961468.
Who is the listed applicant for QUIK-FIL VAPORIZER KEYED FILLER?
The FDA 510(k) record lists Penlon , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QUIK-FIL VAPORIZER KEYED FILLER?
The FDA product code for QUIK-FIL VAPORIZER KEYED FILLER 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 , 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: 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.
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