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FDA 510(k)

AESCULAP TROCAR INSTRUMENT SET

K-Number: K922797 · 1993-03-30

ApplicantAesculap, Inc.
Decision Date1993-03-30
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

AESCULAP TROCAR INSTRUMENT SET is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 1993-03-30 under 510(k) number K922797. 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 AESCULAP TROCAR INSTRUMENT SET?

AESCULAP TROCAR INSTRUMENT SET is a medical device that received FDA 510(k) clearance on 1993-03-30. The listed applicant is Aesculap, Inc.. The 510(k) number is K922797.

When did AESCULAP TROCAR INSTRUMENT SET receive FDA 510(k) clearance?

AESCULAP TROCAR INSTRUMENT SET received FDA 510(k) clearance on 1993-03-30, under 510(k) number K922797.

Who is the listed applicant for AESCULAP TROCAR INSTRUMENT SET?

The FDA 510(k) record lists Aesculap, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AESCULAP TROCAR INSTRUMENT SET?

The FDA product code for AESCULAP TROCAR INSTRUMENT SET is GCJ.

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Other records listing Aesculap, 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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