CLINITRON AT HOME AIR FLUIDED THERAPY
K-Number: K942184 · 1995-02-07
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Device Summary
Frequently Asked Questions
What is the CLINITRON AT HOME AIR FLUIDED THERAPY?
CLINITRON AT HOME AIR FLUIDED THERAPY is a medical device that received FDA 510(k) clearance on 1995-02-07. The listed applicant is Ssi Medical Services, Inc.. The 510(k) number is K942184.
When did CLINITRON AT HOME AIR FLUIDED THERAPY receive FDA 510(k) clearance?
CLINITRON AT HOME AIR FLUIDED THERAPY received FDA 510(k) clearance on 1995-02-07, under 510(k) number K942184.
Who is the listed applicant for CLINITRON AT HOME AIR FLUIDED THERAPY?
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 CLINITRON AT HOME AIR FLUIDED THERAPY?
The FDA product code for CLINITRON AT HOME AIR FLUIDED THERAPY is INX.
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: INX)
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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