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FDA 510(k)

AESCULAP TROCAR COLLAR

K-Number: K941024 · 1994-04-13

ApplicantAesculap, Inc.
Decision Date1994-04-13
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

AESCULAP TROCAR COLLAR is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 1994-04-13 under 510(k) number K941024. 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 COLLAR?

AESCULAP TROCAR COLLAR is a medical device that received FDA 510(k) clearance on 1994-04-13. The listed applicant is Aesculap, Inc.. The 510(k) number is K941024.

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

AESCULAP TROCAR COLLAR received FDA 510(k) clearance on 1994-04-13, under 510(k) number K941024.

Who is the listed applicant for AESCULAP TROCAR COLLAR?

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 COLLAR?

The FDA product code for AESCULAP TROCAR COLLAR 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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