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FDA 510(k)

CASF DRILL GUIDE DG 170

K-Number: K882871 · 1988-09-23

ApplicantTerray Manufacturing, Inc.
Decision Date1988-09-23
Product CodeLYQ
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

CASF DRILL GUIDE DG 170 is the device name listed in this FDA 510(k) record. The listed applicant is Terray Manufacturing, Inc.. It received FDA 510(k) clearance on 1988-09-23 under 510(k) number K882871. The device is classified under product code LYQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the CASF DRILL GUIDE DG 170?

CASF DRILL GUIDE DG 170 is a medical device that received FDA 510(k) clearance on 1988-09-23. The listed applicant is Terray Manufacturing, Inc.. The 510(k) number is K882871.

When did CASF DRILL GUIDE DG 170 receive FDA 510(k) clearance?

CASF DRILL GUIDE DG 170 received FDA 510(k) clearance on 1988-09-23, under 510(k) number K882871.

Who is the listed applicant for CASF DRILL GUIDE DG 170?

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

What is the FDA product code for CASF DRILL GUIDE DG 170?

The FDA product code for CASF DRILL GUIDE DG 170 is LYQ.

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Other records listing Terray Manufacturing, Inc. as applicant

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Related Devices (Code: LYQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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