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)

ARTROMOT K2 CPM

K-Number: K931555 · 1994-01-31

ApplicantOrmed Mfg., Inc.
Decision Date1994-01-31
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ARTROMOT K2 CPM is the device name listed in this FDA 510(k) record. The listed applicant is Ormed Mfg., Inc.. It received FDA 510(k) clearance on 1994-01-31 under 510(k) number K931555. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTROMOT K2 CPM?

ARTROMOT K2 CPM is a medical device that received FDA 510(k) clearance on 1994-01-31. The listed applicant is Ormed Mfg., Inc.. The 510(k) number is K931555.

When did ARTROMOT K2 CPM receive FDA 510(k) clearance?

ARTROMOT K2 CPM received FDA 510(k) clearance on 1994-01-31, under 510(k) number K931555.

Who is the listed applicant for ARTROMOT K2 CPM?

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

What is the FDA product code for ARTROMOT K2 CPM?

The FDA product code for ARTROMOT K2 CPM is BXB.

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 Ormed Mfg., 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.

K882530TAPE STRUNG TONSIL SPONGEK882529BUTCHER STRUNG TONSIL SPONGEK882527GAUZE SPONGEK882528CYLINDRICAL SPONGEK880853CHERRY SPONGEK880851FLAT STICK SPONGE

View all 23 devices →

Related Devices (Code: BXB)

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.

K072887G-TRAINER MEDICALAlter-G, Inc.K003272FLO-BOOTDiscovery Group, LLCK952975ANKLE CALF EXERCISER PHLEBOPUMPPrevent Products, Inc.K953456E-Z FLEXFluid Motion Biotechnologies, Inc.K955106BTE CPM-20Baltimore Therapeutic Equipment Co.K955105BTE CPM-10Baltimore Therapeutic Equipment Co.

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.

↑