VAPOCIDE
K-Number: K970726 · 1998-05-18
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Device Summary
Frequently Asked Questions
What is the VAPOCIDE?
VAPOCIDE is a medical device that received FDA 510(k) clearance on 1998-05-18. The listed applicant is Cottrell, Ltd.. The 510(k) number is K970726.
When did VAPOCIDE receive FDA 510(k) clearance?
VAPOCIDE received FDA 510(k) clearance on 1998-05-18, under 510(k) number K970726.
Who is the listed applicant for VAPOCIDE?
The FDA 510(k) record lists Cottrell, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VAPOCIDE?
The FDA product code for VAPOCIDE is MED.
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 Cottrell, 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: MED)
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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