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FDA 510(k)

HERMES CONTROL CENTER, WITH CONTROL OF THE AESOP 3000HR (HERMES READY).

K-Number: K991444 · 1999-06-25

Decision Date1999-06-25
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HERMES CONTROL CENTER, WITH CONTROL OF THE AESOP 3000HR (HERMES READY). 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 1999-06-25 under 510(k) number K991444. 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 CONTROL CENTER, WITH CONTROL OF THE AESOP 3000HR (HERMES READY).?

HERMES CONTROL CENTER, WITH CONTROL OF THE AESOP 3000HR (HERMES READY). is a medical device that received FDA 510(k) clearance on 1999-06-25. The listed applicant is Computer Motion, Inc.. The 510(k) number is K991444.

When did HERMES CONTROL CENTER, WITH CONTROL OF THE AESOP 3000HR (HERMES READY). receive FDA 510(k) clearance?

HERMES CONTROL CENTER, WITH CONTROL OF THE AESOP 3000HR (HERMES READY). received FDA 510(k) clearance on 1999-06-25, under 510(k) number K991444.

Who is the listed applicant for HERMES CONTROL CENTER, WITH CONTROL OF THE AESOP 3000HR (HERMES READY).?

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 CONTROL CENTER, WITH CONTROL OF THE AESOP 3000HR (HERMES READY).?

The FDA product code for HERMES CONTROL CENTER, WITH CONTROL OF THE AESOP 3000HR (HERMES READY). is GCJ.

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: 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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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