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FDA 510(k)

AUTOZONE

K-Number: K952909 · 1996-03-29

ApplicantHealth Scan, Inc.
Decision Date1996-03-29
Product CodeBZH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AUTOZONE is the device name listed in this FDA 510(k) record. The listed applicant is Health Scan, Inc.. It received FDA 510(k) clearance on 1996-03-29 under 510(k) number K952909. The device is classified under product code BZH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOZONE?

AUTOZONE is a medical device that received FDA 510(k) clearance on 1996-03-29. The listed applicant is Health Scan, Inc.. The 510(k) number is K952909.

When did AUTOZONE receive FDA 510(k) clearance?

AUTOZONE received FDA 510(k) clearance on 1996-03-29, under 510(k) number K952909.

Who is the listed applicant for AUTOZONE?

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

What is the FDA product code for AUTOZONE?

The FDA product code for AUTOZONE is BZH.

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Other records listing Health Scan, 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.

K842634PFLEX RESPIRATORY MUSCLE EXERCISERK820528PFLEX TMK820032VIT-O-METER

Related Devices (Code: BZH)

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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