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FDA 510(k)

ETHICON DRILL BIT AND DRILL GUIDE

K-Number: K944590 · 1995-05-11

ApplicantETHICON, Inc.
Decision Date1995-05-11
Product CodeHSZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ETHICON DRILL BIT AND DRILL GUIDE is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 1995-05-11 under 510(k) number K944590. The device is classified under product code HSZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ETHICON DRILL BIT AND DRILL GUIDE?

ETHICON DRILL BIT AND DRILL GUIDE is a medical device that received FDA 510(k) clearance on 1995-05-11. The listed applicant is ETHICON, Inc.. The 510(k) number is K944590.

When did ETHICON DRILL BIT AND DRILL GUIDE receive FDA 510(k) clearance?

ETHICON DRILL BIT AND DRILL GUIDE received FDA 510(k) clearance on 1995-05-11, under 510(k) number K944590.

Who is the listed applicant for ETHICON DRILL BIT AND DRILL GUIDE?

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

What is the FDA product code for ETHICON DRILL BIT AND DRILL GUIDE?

The FDA product code for ETHICON DRILL BIT AND DRILL GUIDE is HSZ.

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Related Devices (Code: HSZ)

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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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