OXYLATOR EM-100
K-Number: K944349 · 1995-04-17
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Device Summary
Frequently Asked Questions
What is the OXYLATOR EM-100?
OXYLATOR EM-100 is a medical device that received FDA 510(k) clearance on 1995-04-17. The listed applicant is Cpr Medical Devices, Inc.. The 510(k) number is K944349.
When did OXYLATOR EM-100 receive FDA 510(k) clearance?
OXYLATOR EM-100 received FDA 510(k) clearance on 1995-04-17, under 510(k) number K944349.
Who is the listed applicant for OXYLATOR EM-100?
The FDA 510(k) record lists Cpr Medical Devices, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OXYLATOR EM-100?
The FDA product code for OXYLATOR EM-100 is BTL.
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.
Related Devices (Code: BTL)
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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