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FDA 510(k)

CLINITRON C-II

K-Number: K920112 · 1992-01-24

ApplicantSupport Systems Intl.
Decision Date1992-01-24
Product CodeINX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CLINITRON C-II is the device name listed in this FDA 510(k) record. The listed applicant is Support Systems Intl.. It received FDA 510(k) clearance on 1992-01-24 under 510(k) number K920112. 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 C-II?

CLINITRON C-II is a medical device that received FDA 510(k) clearance on 1992-01-24. The listed applicant is Support Systems Intl.. The 510(k) number is K920112.

When did CLINITRON C-II receive FDA 510(k) clearance?

CLINITRON C-II received FDA 510(k) clearance on 1992-01-24, under 510(k) number K920112.

Who is the listed applicant for CLINITRON C-II?

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 CLINITRON C-II?

The FDA product code for CLINITRON C-II 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K941610CLENSICAIR LOW AIRLOSS HYDROTHERAPYK940662I-5000K922973RESTCUE CCK920382FLEXICAIR LOW AIRLOSS THERAPY UNIT

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.

K972176HOME CARE BEAD BEDKinetic Concepts, Inc.K964223CLINITRON RITE-HITEHill-Rom, Inc.K943385CLINITRON ELEXISSsi Medical Services, Inc.K942184CLINITRON AT HOME AIR FLUIDED THERAPYSsi Medical Services, Inc.K931168X-20 AIR SUPPORT BEDAmerican Life Support Technology, Inc.K934689LOW AIR LOSS MATTRESS, MODIFICATIONCardio Systems, Inc.

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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