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FDA 510(k)

AESOP SYSTEM AND ACCESSORIES

K-Number: K963126 · 1997-04-07

ApplicantComputer Motion, Inc.
Decision Date1997-04-07
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

AESOP SYSTEM AND ACCESSORIES 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 1997-04-07 under 510(k) number K963126. 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 AESOP SYSTEM AND ACCESSORIES?

AESOP SYSTEM AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1997-04-07. The listed applicant is Computer Motion, Inc.. The 510(k) number is K963126.

When did AESOP SYSTEM AND ACCESSORIES receive FDA 510(k) clearance?

AESOP SYSTEM AND ACCESSORIES received FDA 510(k) clearance on 1997-04-07, under 510(k) number K963126.

Who is the listed applicant for AESOP SYSTEM AND ACCESSORIES?

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 AESOP SYSTEM AND ACCESSORIES?

The FDA product code for AESOP SYSTEM AND ACCESSORIES is GCJ.

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Other records listing Computer Motion, Inc. as applicant

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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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