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FDA 510(k)

AUTO-LOCK

K-Number: K010477 · 2001-10-09

ApplicantAuto-Lock
Decision Date2001-10-09
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AUTO-LOCK is the device name listed in this FDA 510(k) record. The listed applicant is Auto-Lock. It received FDA 510(k) clearance on 2001-10-09 under 510(k) number K010477. The device is classified under product code MEG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO-LOCK?

AUTO-LOCK is a medical device that received FDA 510(k) clearance on 2001-10-09. The listed applicant is Auto-Lock. The 510(k) number is K010477.

When did AUTO-LOCK receive FDA 510(k) clearance?

AUTO-LOCK received FDA 510(k) clearance on 2001-10-09, under 510(k) number K010477.

Who is the listed applicant for AUTO-LOCK?

The FDA 510(k) record lists Auto-Lock as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUTO-LOCK?

The FDA product code for AUTO-LOCK is MEG.

Related Devices (Code: MEG)

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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