Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ROTO REST KINETIC TREATMENT TABLE PEDIA

K-Number: K822402 · 1982-10-22

ApplicantKinetic Concepts, Inc.
Decision Date1982-10-22
Product CodeIKZ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ROTO REST KINETIC TREATMENT TABLE PEDIA is the device name listed in this FDA 510(k) record. The listed applicant is Kinetic Concepts, Inc.. It received FDA 510(k) clearance on 1982-10-22 under 510(k) number K822402. The device is classified under product code IKZ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROTO REST KINETIC TREATMENT TABLE PEDIA?

ROTO REST KINETIC TREATMENT TABLE PEDIA is a medical device that received FDA 510(k) clearance on 1982-10-22. The listed applicant is Kinetic Concepts, Inc.. The 510(k) number is K822402.

When did ROTO REST KINETIC TREATMENT TABLE PEDIA receive FDA 510(k) clearance?

ROTO REST KINETIC TREATMENT TABLE PEDIA received FDA 510(k) clearance on 1982-10-22, under 510(k) number K822402.

Who is the listed applicant for ROTO REST KINETIC TREATMENT TABLE PEDIA?

The FDA 510(k) record lists Kinetic Concepts, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ROTO REST KINETIC TREATMENT TABLE PEDIA?

The FDA product code for ROTO REST KINETIC TREATMENT TABLE PEDIA is IKZ.

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 Kinetic Concepts, 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.

K050261V.A.C. GRANUFOAM SILVER PROTECTION DRESSINGK041642V.A.C. GRANUFOAM SILVER DRESSINGK032310MINI V.A.C., V.A.C. FREEDOM, V.A.C. ATSK022011V.A.C. ABDOMINAL DRESSINGK021500VACUUM ASSISTED CLOSUREK021501V.A.C. INSTILLAMAT (VACUUM ASSISTED CLOSURE INSTILLAMAT

View all 48 devices →

Related Devices (Code: IKZ)

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.

K972486PRESSUREGUARD IVSpan-America Medical Systems, Inc.K972111RUMORS DYNAMIC AIR THERAPY UNITHill-Rom, Inc.K962788CLINIDYNE ROTATIONAL THERAPY MATTRESS SYSTEMGaymar Industries, Inc.K954671THE FREEDOM BEDProbed Medical Technologies, Inc.K950756PULMONEX DYNAMIC AIR THERAPY UNITHill-Rom, Inc.K950681MODEL TURN Q PLUS AUTOMATIC TURNING MATTRESS WITH LOW AIR LOSS THERAPYInvacare Corp.

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.

↑