ACUCAIR CUSHION CONTINUOUS AIRFLOW SYSTEM
K-Number: K882161 · 1988-07-12
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Device Summary
Frequently Asked Questions
What is the ACUCAIR CUSHION CONTINUOUS AIRFLOW SYSTEM?
ACUCAIR CUSHION CONTINUOUS AIRFLOW SYSTEM is a medical device that received FDA 510(k) clearance on 1988-07-12. The listed applicant is Ssi Medical Services, Inc.. The 510(k) number is K882161.
When did ACUCAIR CUSHION CONTINUOUS AIRFLOW SYSTEM receive FDA 510(k) clearance?
ACUCAIR CUSHION CONTINUOUS AIRFLOW SYSTEM received FDA 510(k) clearance on 1988-07-12, under 510(k) number K882161.
Who is the listed applicant for ACUCAIR CUSHION CONTINUOUS AIRFLOW SYSTEM?
The FDA 510(k) record lists Ssi Medical Services, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACUCAIR CUSHION CONTINUOUS AIRFLOW SYSTEM?
The FDA product code for ACUCAIR CUSHION CONTINUOUS AIRFLOW SYSTEM is FNM.
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 Ssi Medical Services, 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: FNM)
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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