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FDA 510(k)

TUBING CLAMP CAT#1000-A

K-Number: K854512 · 1985-12-02

ApplicantRao Medical Devices, Inc.
Decision Date1985-12-02
Product CodeFKK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TUBING CLAMP CAT#1000-A is the device name listed in this FDA 510(k) record. The listed applicant is Rao Medical Devices, Inc.. It received FDA 510(k) clearance on 1985-12-02 under 510(k) number K854512. The device is classified under product code FKK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUBING CLAMP CAT#1000-A?

TUBING CLAMP CAT#1000-A is a medical device that received FDA 510(k) clearance on 1985-12-02. The listed applicant is Rao Medical Devices, Inc.. The 510(k) number is K854512.

When did TUBING CLAMP CAT#1000-A receive FDA 510(k) clearance?

TUBING CLAMP CAT#1000-A received FDA 510(k) clearance on 1985-12-02, under 510(k) number K854512.

Who is the listed applicant for TUBING CLAMP CAT#1000-A?

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

What is the FDA product code for TUBING CLAMP CAT#1000-A?

The FDA product code for TUBING CLAMP CAT#1000-A is FKK.

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 Rao Medical Devices, 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.

K854965IN LINE VALVE CATALOG NO. 2000A

Related Devices (Code: FKK)

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.

K854517NEW TRAVENOL ROLLER CLAMP-SOLUTION ADMIN. SETTravenol Laboratories, S.A.K844121CLAMP, TUBING, LINEDyn-A-Med ProductsK831689EMPTY DIALYSATE CONTAINERDelmed, Inc.K822551AMP CAPD UNISPIKE AMINISTRATION SETAmerican Medical Products, Inc.K802009FLOWCLAMP CAT.#1011 & 1012Pollak (Intl.), Ltd.

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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