CLENSICAIR LOW AIRLOSS HYDROTHERAPY
K-Number: K941610 · 1995-02-10
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Device Summary
Frequently Asked Questions
What is the CLENSICAIR LOW AIRLOSS HYDROTHERAPY?
CLENSICAIR LOW AIRLOSS HYDROTHERAPY is a medical device that received FDA 510(k) clearance on 1995-02-10. The listed applicant is Support Systems Intl.. The 510(k) number is K941610.
When did CLENSICAIR LOW AIRLOSS HYDROTHERAPY receive FDA 510(k) clearance?
CLENSICAIR LOW AIRLOSS HYDROTHERAPY received FDA 510(k) clearance on 1995-02-10, under 510(k) number K941610.
Who is the listed applicant for CLENSICAIR LOW AIRLOSS HYDROTHERAPY?
The FDA 510(k) record lists Support Systems Intl. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CLENSICAIR LOW AIRLOSS HYDROTHERAPY?
The FDA product code for CLENSICAIR LOW AIRLOSS HYDROTHERAPY is IOQ.
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 Support Systems Intl. 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: IOQ)
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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