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FDA 510(k)

SOCRATES ROBOTIC TELEMONITORING SYSTEM

K-Number: K003661 · 2001-10-05

Decision Date2001-10-05
Product CodeNEQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SOCRATES ROBOTIC TELEMONITORING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Computer Motion, Inc.. It received FDA 510(k) clearance on 2001-10-05 under 510(k) number K003661. The device is classified under product code NEQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOCRATES ROBOTIC TELEMONITORING SYSTEM?

SOCRATES ROBOTIC TELEMONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 2001-10-05. The listed applicant is Computer Motion, Inc.. The 510(k) number is K003661.

When did SOCRATES ROBOTIC TELEMONITORING SYSTEM receive FDA 510(k) clearance?

SOCRATES ROBOTIC TELEMONITORING SYSTEM received FDA 510(k) clearance on 2001-10-05, under 510(k) number K003661.

Who is the listed applicant for SOCRATES ROBOTIC TELEMONITORING SYSTEM?

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

What is the FDA product code for SOCRATES ROBOTIC TELEMONITORING SYSTEM?

The FDA product code for SOCRATES ROBOTIC TELEMONITORING SYSTEM is NEQ.

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.

Other records listing Computer Motion, 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.

View all 26 devices →

Related Devices (Code: NEQ)

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.

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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