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FDA 510(k)

RNET SYSTEM, IV RECEIVING TERMINAL, TRANSMITTER

K-Number: K863716 · 1986-12-22

ApplicantFuturecare Systems, Inc.
Decision Date1986-12-22
Product Code
DecisionSubstantially Equivalent

Device Summary

RNET SYSTEM, IV RECEIVING TERMINAL, TRANSMITTER is the device name listed in this FDA 510(k) record. The listed applicant is Futurecare Systems, Inc.. It received FDA 510(k) clearance on 1986-12-22 under 510(k) number K863716. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RNET SYSTEM, IV RECEIVING TERMINAL, TRANSMITTER?

RNET SYSTEM, IV RECEIVING TERMINAL, TRANSMITTER is a medical device that received FDA 510(k) clearance on 1986-12-22. The listed applicant is Futurecare Systems, Inc.. The 510(k) number is K863716.

When did RNET SYSTEM, IV RECEIVING TERMINAL, TRANSMITTER receive FDA 510(k) clearance?

RNET SYSTEM, IV RECEIVING TERMINAL, TRANSMITTER received FDA 510(k) clearance on 1986-12-22, under 510(k) number K863716.

Who is the listed applicant for RNET SYSTEM, IV RECEIVING TERMINAL, TRANSMITTER?

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

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 Futurecare Systems, 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.

K903512FUTURECARE CARELYNK IV SYSTEMK871944FUTURECARE CARELYNK SYSTEM (ENTIRE SYSTEM)

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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