Hermes Operating Room Control Center with the Wom 20l Insufflator

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K980787 ↗

FDA Product Code

GCJ

Device Class

Class II

Regulation

21 CFR Part 876.1500

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

• Hermes O.R. Control Center Modification

  Class II

  FDA 510(k) K031956 Active Cleared 17 Jul 2003

• Aesop System and Accessories

  Class II

  FDA 510(k) K960655 Active Cleared 3 May 1996

• Hermes Control Center, with Control of the Aesop 3000HR (Hermes Ready).

  Class II

  FDA 510(k) K991444 Active Cleared 25 Jun 1999

• Zeus Microwrist Robotic Surgical System

  Class II

  FDA 510(k) K013551 Active Cleared 28 Mar 2002

• Modification to Hermes Operating Room Control Center

  Class II

  FDA 510(k) K003222 Active Cleared 3 Nov 2000

• Modification to Hermes O.R. Control Center

  Class II

  FDA 510(k) K031720 Active Cleared 11 Jul 2003

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