DISPOSA-HOOD
K-Number: K792144 · 1979-12-05
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Device Summary
Frequently Asked Questions
What is the DISPOSA-HOOD?
DISPOSA-HOOD is a medical device that received FDA 510(k) clearance on 1979-12-05. The listed applicant is Utah Medical Products, Inc.. The 510(k) number is K792144.
When did DISPOSA-HOOD receive FDA 510(k) clearance?
DISPOSA-HOOD received FDA 510(k) clearance on 1979-12-05, under 510(k) number K792144.
Who is the listed applicant for DISPOSA-HOOD?
The FDA 510(k) record lists Utah Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISPOSA-HOOD?
The FDA product code for DISPOSA-HOOD is FOG.
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 Utah Medical Products, 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: FOG)
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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