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FDA 510(k)

MODIFICATION TO HERMES O.R. CONTROL CENTER

K-Number: K031382 · 2003-06-30

ApplicantComputer Motion, Inc.
Decision Date2003-06-30
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO HERMES O.R. 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 2003-06-30 under 510(k) number K031382. 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 MODIFICATION TO HERMES O.R. CONTROL CENTER?

MODIFICATION TO HERMES O.R. CONTROL CENTER is a medical device that received FDA 510(k) clearance on 2003-06-30. The listed applicant is Computer Motion, Inc.. The 510(k) number is K031382.

When did MODIFICATION TO HERMES O.R. CONTROL CENTER receive FDA 510(k) clearance?

MODIFICATION TO HERMES O.R. CONTROL CENTER received FDA 510(k) clearance on 2003-06-30, under 510(k) number K031382.

Who is the listed applicant for MODIFICATION TO HERMES O.R. 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 MODIFICATION TO HERMES O.R. CONTROL CENTER?

The FDA product code for MODIFICATION TO HERMES O.R. 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 CENTERK030578BIPOLAR GRASPER AND BIPOLAR SCISSORS FOR THE ZEUS MICROWRIST SURGICAL SYSTEMK030718SCB COMPUTER MOTION INTERFACE CONTROLLERK030240MODIFICATION TO HERMES OPERATING ROOM CONTROL CENTERK024294MODIFICATION TO HERMES OPERATING ROOM CONTROL CENTER

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Related Devices (Code: GCJ)

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.

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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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