ATMOS ENT CABINET PRACTICA 3
K-Number: K791935 · 1979-10-30
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Device Summary
Frequently Asked Questions
What is the ATMOS ENT CABINET PRACTICA 3?
ATMOS ENT CABINET PRACTICA 3 is a medical device that received FDA 510(k) clearance on 1979-10-30. The listed applicant is Jedmed Instrument Co.. The 510(k) number is K791935.
When did ATMOS ENT CABINET PRACTICA 3 receive FDA 510(k) clearance?
ATMOS ENT CABINET PRACTICA 3 received FDA 510(k) clearance on 1979-10-30, under 510(k) number K791935.
Who is the listed applicant for ATMOS ENT CABINET PRACTICA 3?
The FDA 510(k) record lists Jedmed Instrument Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ATMOS ENT CABINET PRACTICA 3?
The FDA product code for ATMOS ENT CABINET PRACTICA 3 is ETF.
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 Jedmed Instrument Co. 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: ETF)
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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