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Hermes Operating Room Control Center

by Computer Motion, Inc. 3 variants

510(k) K973700

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK973700 Date24 Feb 1998ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
GCJ
Device Class
Class II
Regulation
21 CFR Part 876.1500
Advisory Committee
Gastroenterology, Urology
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 23 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The Hermes Operating Room Control Center is a device designed for use in the operating room environment. It serves as a centralized control system for managing various operating room functions.

This device is supplied as a non-sterile, reusable system intended for use in healthcare facilities. It does not have MRI safety information specified in the data, and its use, storage, and handling should follow manufacturer guidelines. The device received traditional 510(k) clearance (K973700) from the FDA, with a decision date of February 24, 1998, and is classified under product code GCJ.

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