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FDA 510(k)

CLINITRON AT HOME AIR FLUIDED THERAPY

K-Number: K942184 · 1995-02-07

Decision Date1995-02-07
Product CodeINX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CLINITRON AT HOME AIR FLUIDED THERAPY is the device name listed in this FDA 510(k) record. The listed applicant is Ssi Medical Services, Inc.. It received FDA 510(k) clearance on 1995-02-07 under 510(k) number K942184. The device is classified under product code INX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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