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FDA 510(k)

ELS AUTOMATIC TUBING CLAMP SYSTEM

K-Number: K921993 · 1994-01-05

ApplicantRocky Mountain Research, Inc.
Decision Date1994-01-05
Product CodeFIG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ELS AUTOMATIC TUBING CLAMP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Rocky Mountain Research, Inc.. It received FDA 510(k) clearance on 1994-01-05 under 510(k) number K921993. The device is classified under product code FIG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELS AUTOMATIC TUBING CLAMP SYSTEM?

ELS AUTOMATIC TUBING CLAMP SYSTEM is a medical device that received FDA 510(k) clearance on 1994-01-05. The listed applicant is Rocky Mountain Research, Inc.. The 510(k) number is K921993.

When did ELS AUTOMATIC TUBING CLAMP SYSTEM receive FDA 510(k) clearance?

ELS AUTOMATIC TUBING CLAMP SYSTEM received FDA 510(k) clearance on 1994-01-05, under 510(k) number K921993.

Who is the listed applicant for ELS AUTOMATIC TUBING CLAMP SYSTEM?

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

What is the FDA product code for ELS AUTOMATIC TUBING CLAMP SYSTEM?

The FDA product code for ELS AUTOMATIC TUBING CLAMP SYSTEM is FIG.

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 Rocky Mountain Research, 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.

K992857LEVELSENS - FLEXIBLE, MODEL 201110, LEVELSENS - RIGID, MODEL 201070K961364AUTOMATIC TUBING CLAMP SYSTEM (ATC)K961598ELS AUTOMATIC TUBING CLAMP SYSTEMK914459AUTOMATIC TUBING CLAMP

Related Devices (Code: FIG)

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.

K093915DEKA TAC DEVICEDeka Research & Development Corp.K914459AUTOMATIC TUBING CLAMPRocky Mountain Research, Inc.K770535C-DAK 3500Cordis Corp.

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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