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FDA 510(k)

AUTOMATIC TUBING CLAMP

K-Number: K914459 · 1992-06-24

ApplicantRocky Mountain Research, Inc.
Decision Date1992-06-24
Product CodeFIG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

AUTOMATIC TUBING CLAMP 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 1992-06-24 under 510(k) number K914459. 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 AUTOMATIC TUBING CLAMP?

AUTOMATIC TUBING CLAMP is a medical device that received FDA 510(k) clearance on 1992-06-24. The listed applicant is Rocky Mountain Research, Inc.. The 510(k) number is K914459.

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

AUTOMATIC TUBING CLAMP received FDA 510(k) clearance on 1992-06-24, under 510(k) number K914459.

Who is the listed applicant for AUTOMATIC TUBING CLAMP?

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 AUTOMATIC TUBING CLAMP?

The FDA product code for AUTOMATIC TUBING CLAMP 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 SYSTEMK921993ELS AUTOMATIC TUBING CLAMP SYSTEM

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.K921993ELS AUTOMATIC TUBING CLAMP SYSTEMRocky 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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