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FDA 510(k)

AESCULAP BIOPOLAR COAGULATOR

K-Number: K952524 · 1995-06-29

ApplicantAesculap, Inc.
Decision Date1995-06-29
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AESCULAP BIOPOLAR COAGULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 1995-06-29 under 510(k) number K952524. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AESCULAP BIOPOLAR COAGULATOR?

AESCULAP BIOPOLAR COAGULATOR is a medical device that received FDA 510(k) clearance on 1995-06-29. The listed applicant is Aesculap, Inc.. The 510(k) number is K952524.

When did AESCULAP BIOPOLAR COAGULATOR receive FDA 510(k) clearance?

AESCULAP BIOPOLAR COAGULATOR received FDA 510(k) clearance on 1995-06-29, under 510(k) number K952524.

Who is the listed applicant for AESCULAP BIOPOLAR COAGULATOR?

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 BIOPOLAR COAGULATOR?

The FDA product code for AESCULAP BIOPOLAR COAGULATOR is GEI.

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Other records listing Aesculap, Inc. as applicant

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Related Devices (Code: GEI)

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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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