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FDA 510(k)

KEY DRILL

K-Number: K821127 · 1982-06-03

ApplicantKey Medical, Inc.
Decision Date1982-06-03
Product CodeGFG
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KEY DRILL is the device name listed in this FDA 510(k) record. The listed applicant is Key Medical, Inc.. It received FDA 510(k) clearance on 1982-06-03 under 510(k) number K821127. The device is classified under product code GFG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KEY DRILL?

KEY DRILL is a medical device that received FDA 510(k) clearance on 1982-06-03. The listed applicant is Key Medical, Inc.. The 510(k) number is K821127.

When did KEY DRILL receive FDA 510(k) clearance?

KEY DRILL received FDA 510(k) clearance on 1982-06-03, under 510(k) number K821127.

Who is the listed applicant for KEY DRILL?

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

What is the FDA product code for KEY DRILL?

The FDA product code for KEY DRILL is GFG.

Related Clinical Trials

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Other records listing Key Medical, Inc. as applicant

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.

K812760HI-TEMP CARDIOVASCULAR CAUTERYK812644REPLACEABLE BATTERY PERFECTEMP 2 CAUTK810909MICRO CAUTERY

Related Devices (Code: GFG)

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.

K935225MITEK MODULAR DRILL BITMitek Surgical Products, Inc.K821486MICRO DRILLSSpire Medical, Inc.

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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