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FDA 510(k)

HERMES OPERATING ROOM CONTROL CENTER

K-Number: K990691 · 1999-03-23

ApplicantComputer Motion, Inc.
Decision Date1999-03-23
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HERMES OPERATING ROOM CONTROL CENTER 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 1999-03-23 under 510(k) number K990691. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HERMES OPERATING ROOM CONTROL CENTER?

HERMES OPERATING ROOM CONTROL CENTER is a medical device that received FDA 510(k) clearance on 1999-03-23. The listed applicant is Computer Motion, Inc.. The 510(k) number is K990691.

When did HERMES OPERATING ROOM CONTROL CENTER receive FDA 510(k) clearance?

HERMES OPERATING ROOM CONTROL CENTER received FDA 510(k) clearance on 1999-03-23, under 510(k) number K990691.

Who is the listed applicant for HERMES OPERATING ROOM CONTROL CENTER?

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 HERMES OPERATING ROOM CONTROL CENTER?

The FDA product code for HERMES OPERATING ROOM CONTROL CENTER is GCJ.

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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.

K031956MODIFICATION TO HERMES O.R. CONTROL CENTERK031720MODIFICATION TO HERMES O.R. CONTROL CENTERK031382MODIFICATION TO HERMES O.R. CONTROL CENTERK030578BIPOLAR GRASPER AND BIPOLAR SCISSORS FOR THE ZEUS MICROWRIST SURGICAL SYSTEMK030718SCB COMPUTER MOTION INTERFACE CONTROLLERK030240MODIFICATION TO HERMES OPERATING ROOM CONTROL CENTER

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Related Devices (Code: GCJ)

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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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