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FDA 510(k)

MOTOR DRIVEN EXTIRPATION INSTRUMENTS

K-Number: K904859 · 1991-03-15

ApplicantAesculap, Inc.
Decision Date1991-03-15
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MOTOR DRIVEN EXTIRPATION INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 1991-03-15 under 510(k) number K904859. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOTOR DRIVEN EXTIRPATION INSTRUMENTS?

MOTOR DRIVEN EXTIRPATION INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1991-03-15. The listed applicant is Aesculap, Inc.. The 510(k) number is K904859.

When did MOTOR DRIVEN EXTIRPATION INSTRUMENTS receive FDA 510(k) clearance?

MOTOR DRIVEN EXTIRPATION INSTRUMENTS received FDA 510(k) clearance on 1991-03-15, under 510(k) number K904859.

Who is the listed applicant for MOTOR DRIVEN EXTIRPATION INSTRUMENTS?

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 MOTOR DRIVEN EXTIRPATION INSTRUMENTS?

The FDA product code for MOTOR DRIVEN EXTIRPATION INSTRUMENTS is HRX.

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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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