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FDA 510(k)

HAND DRILL, MODEL 11-9901-7

K-Number: K022712 · 2002-11-12

ApplicantMedical Design, LLC
Decision Date2002-11-12
Product CodeHBG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

HAND DRILL, MODEL 11-9901-7 is the device name listed in this FDA 510(k) record. The listed applicant is Medical Design, LLC. It received FDA 510(k) clearance on 2002-11-12 under 510(k) number K022712. The device is classified under product code HBG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HAND DRILL, MODEL 11-9901-7?

HAND DRILL, MODEL 11-9901-7 is a medical device that received FDA 510(k) clearance on 2002-11-12. The listed applicant is Medical Design, LLC. The 510(k) number is K022712.

When did HAND DRILL, MODEL 11-9901-7 receive FDA 510(k) clearance?

HAND DRILL, MODEL 11-9901-7 received FDA 510(k) clearance on 2002-11-12, under 510(k) number K022712.

Who is the listed applicant for HAND DRILL, MODEL 11-9901-7?

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

What is the FDA product code for HAND DRILL, MODEL 11-9901-7?

The FDA product code for HAND DRILL, MODEL 11-9901-7 is HBG.

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Other records listing Medical Design, LLC as applicant

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Related Devices (Code: HBG)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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