VIGGO INSUFLON
K-Number: K881767 · 1988-08-24
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Device Summary
Frequently Asked Questions
What is the VIGGO INSUFLON?
VIGGO INSUFLON is a medical device that received FDA 510(k) clearance on 1988-08-24. The listed applicant is Ohmeda Medical. The 510(k) number is K881767.
When did VIGGO INSUFLON receive FDA 510(k) clearance?
VIGGO INSUFLON received FDA 510(k) clearance on 1988-08-24, under 510(k) number K881767.
Who is the listed applicant for VIGGO INSUFLON?
The FDA 510(k) record lists Ohmeda Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VIGGO INSUFLON?
The FDA product code for VIGGO INSUFLON is FOZ.
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 Ohmeda Medical 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: FOZ)
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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