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)

RMI SOFCLAMP

K-Number: K920676 · 1992-04-15

ApplicantResearch Medical, Inc.
Decision Date1992-04-15
Product CodeDSS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RMI SOFCLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Research Medical, Inc.. It received FDA 510(k) clearance on 1992-04-15 under 510(k) number K920676. The device is classified under product code DSS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RMI SOFCLAMP?

RMI SOFCLAMP is a medical device that received FDA 510(k) clearance on 1992-04-15. The listed applicant is Research Medical, Inc.. The 510(k) number is K920676.

When did RMI SOFCLAMP receive FDA 510(k) clearance?

RMI SOFCLAMP received FDA 510(k) clearance on 1992-04-15, under 510(k) number K920676.

Who is the listed applicant for RMI SOFCLAMP?

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

What is the FDA product code for RMI SOFCLAMP?

The FDA product code for RMI SOFCLAMP is DSS.

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 Research Medical, 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.

K970739RMI HEMOCONCENTRATOR PREFERENCE PACKK964833RMI DUAL FLUID IRRIGATING SYRINGEK961927RMI HEMOCONCENTRACTOR TUBING SETK960098RMI INTERNAL MAMMARY ARTERY CANNULAK951344RMI HEMOCONCENTRATORK922083RMI SURGICCAL SITE VISUALIZATION WAND

View all 35 devices →

Related Devices (Code: DSS)

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.

K983744MCAS (MODULAR CLIP APPLIER SYSTEM)Applied Medical ResourcesK961333HEARTPORT MULTIFIRE CLIP APPLIERHeartport, Inc.K920104IDENTI LOOPS DEGANIA SILICONEPuritas Health Care, Inc.K914523CRI VESSEL OCCLUSIN SYSTEM/CRI OCCLUSION COILCatheter Research C/O Burditt, Bowles & RadziusK901303HORIZON SURGICAL LIGATING AND MARKING CLIPHorizon Surgical, Inc.K883909SURGICAL SPRING CLIPSApplied Vascular Devices, 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.

↑