APEX MEDICAL MOBINEB, 9R-027 SERIES
K-Number: K070990 · 2007-05-18
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Device Summary
Frequently Asked Questions
What is the APEX MEDICAL MOBINEB, 9R-027 SERIES?
APEX MEDICAL MOBINEB, 9R-027 SERIES is a medical device that received FDA 510(k) clearance on 2007-05-18. The listed applicant is Apex Medical Corp.. The 510(k) number is K070990.
When did APEX MEDICAL MOBINEB, 9R-027 SERIES receive FDA 510(k) clearance?
APEX MEDICAL MOBINEB, 9R-027 SERIES received FDA 510(k) clearance on 2007-05-18, under 510(k) number K070990.
Who is the listed applicant for APEX MEDICAL MOBINEB, 9R-027 SERIES?
The FDA 510(k) record lists Apex Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for APEX MEDICAL MOBINEB, 9R-027 SERIES?
The FDA product code for APEX MEDICAL MOBINEB, 9R-027 SERIES is CAF.
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 Apex Medical Corp. 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: CAF)
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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