FREEDOM OXIMETER/EEG DIGITAL INTERFACE
K-Number: K924752 · 1993-09-10
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Device Summary
Frequently Asked Questions
What is the FREEDOM OXIMETER/EEG DIGITAL INTERFACE?
FREEDOM OXIMETER/EEG DIGITAL INTERFACE is a medical device that received FDA 510(k) clearance on 1993-09-10. The listed applicant is Pro-Tech, Inc.. The 510(k) number is K924752.
When did FREEDOM OXIMETER/EEG DIGITAL INTERFACE receive FDA 510(k) clearance?
FREEDOM OXIMETER/EEG DIGITAL INTERFACE received FDA 510(k) clearance on 1993-09-10, under 510(k) number K924752.
Who is the listed applicant for FREEDOM OXIMETER/EEG DIGITAL INTERFACE?
The FDA 510(k) record lists Pro-Tech, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FREEDOM OXIMETER/EEG DIGITAL INTERFACE?
The FDA product code for FREEDOM OXIMETER/EEG DIGITAL INTERFACE is DQA.
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 Pro-Tech, 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: DQA)
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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