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FDA 510(k)

CAREMOR CLINER

K-Number: K941569 · 1994-04-26

ApplicantWinco, Inc.
Decision Date1994-04-26
Product CodeINM
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CAREMOR CLINER is the device name listed in this FDA 510(k) record. The listed applicant is Winco, Inc.. It received FDA 510(k) clearance on 1994-04-26 under 510(k) number K941569. The device is classified under product code INM. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAREMOR CLINER?

CAREMOR CLINER is a medical device that received FDA 510(k) clearance on 1994-04-26. The listed applicant is Winco, Inc.. The 510(k) number is K941569.

When did CAREMOR CLINER receive FDA 510(k) clearance?

CAREMOR CLINER received FDA 510(k) clearance on 1994-04-26, under 510(k) number K941569.

Who is the listed applicant for CAREMOR CLINER?

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

What is the FDA product code for CAREMOR CLINER?

The FDA product code for CAREMOR CLINER is INM.

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 Winco, 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.

K080533WINCO MODEL POWER SERIES LIFT CHAIRK933000RECLINING GERI CHAIRS W/CASTERS & LAP TRAY

Related Devices (Code: INM)

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.

K063521NISSIN PEDIATRIC SERIES WHEELCHAIRNissin Medical, Inc.K941738STRYKER 5050 STRECHAIRStryker MedicalK933000RECLINING GERI CHAIRS W/CASTERS & LAP TRAYWinco, Inc.K926028BENCHESTheradapt Products, Inc.K926054ELD-ARONDAK CHAIRAl'S Woodcraft, Inc.K926053ELD-ARONDAK CHAIRAlert Care, 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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