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FDA 510(k)

RESTCUE CC

K-Number: K922973 · 1992-07-30

ApplicantSupport Systems Intl.
Decision Date1992-07-30
Product CodeIOQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RESTCUE CC 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 1992-07-30 under 510(k) number K922973. The device is classified under product code IOQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESTCUE CC?

RESTCUE CC is a medical device that received FDA 510(k) clearance on 1992-07-30. The listed applicant is Support Systems Intl.. The 510(k) number is K922973.

When did RESTCUE CC receive FDA 510(k) clearance?

RESTCUE CC received FDA 510(k) clearance on 1992-07-30, under 510(k) number K922973.

Who is the listed applicant for RESTCUE CC?

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 RESTCUE CC?

The FDA product code for RESTCUE CC 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.

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-5000K920382FLEXICAIR LOW AIRLOSS THERAPY UNITK920112CLINITRON C-II

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.

K122473TOTALCARE SPOT TOTALCARE BARIATRIC TOTALCARE DUO TOATALCARE BED SYSTEM TOTALCARE DUO2Hill-RomK973624NURSE'S AID PATIENT ROTATION SYSTEMAir Med Assist ProductsK970364AIRTEC2 LOW AIR LOSS THERAPY BEDApex Metal, Inc.K970363HYDROTEC LOW AIR LOSS THERAPY BEDApex Metal, Inc.K970636TOTALCARE., MODULAR THERAPY SYSTEM (MTS)Hill-Rom, Inc.K964873SILKAIR LOW AIRLOSS THERAPYHill-Rom, Inc.

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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