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FDA 510(k)

AESCULAP MINOP SYSTEM

K-Number: K983365 · 1998-12-18

ApplicantAesculap, Inc.
Decision Date1998-12-18
Product CodeGWG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

AESCULAP MINOP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 1998-12-18 under 510(k) number K983365. The device is classified under product code GWG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AESCULAP MINOP SYSTEM?

AESCULAP MINOP SYSTEM is a medical device that received FDA 510(k) clearance on 1998-12-18. The listed applicant is Aesculap, Inc.. The 510(k) number is K983365.

When did AESCULAP MINOP SYSTEM receive FDA 510(k) clearance?

AESCULAP MINOP SYSTEM received FDA 510(k) clearance on 1998-12-18, under 510(k) number K983365.

Who is the listed applicant for AESCULAP MINOP SYSTEM?

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 MINOP SYSTEM?

The FDA product code for AESCULAP MINOP SYSTEM is GWG.

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Other records listing Aesculap, Inc. as applicant

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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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