GAS-VAK(R), MODEL 300
K-Number: K890438 · 1989-08-07
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Device Summary
Frequently Asked Questions
What is the GAS-VAK(R), MODEL 300?
GAS-VAK(R), MODEL 300 is a medical device that received FDA 510(k) clearance on 1989-08-07. The listed applicant is Gas-Vak. The 510(k) number is K890438.
When did GAS-VAK(R), MODEL 300 receive FDA 510(k) clearance?
GAS-VAK(R), MODEL 300 received FDA 510(k) clearance on 1989-08-07, under 510(k) number K890438.
Who is the listed applicant for GAS-VAK(R), MODEL 300?
The FDA 510(k) record lists Gas-Vak as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GAS-VAK(R), MODEL 300?
The FDA product code for GAS-VAK(R), MODEL 300 is CBN.
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 Gas-Vak 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: CBN)
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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