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FDA 510(k)

STERI-AID KIT

K-Number: K963049 · 1996-11-12

ApplicantSteri-Aid, Inc.
Decision Date1996-11-12
Product CodeFQZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERI-AID KIT is the device name listed in this FDA 510(k) record. The listed applicant is Steri-Aid, Inc.. It received FDA 510(k) clearance on 1996-11-12 under 510(k) number K963049. The device is classified under product code FQZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERI-AID KIT?

STERI-AID KIT is a medical device that received FDA 510(k) clearance on 1996-11-12. The listed applicant is Steri-Aid, Inc.. The 510(k) number is K963049.

When did STERI-AID KIT receive FDA 510(k) clearance?

STERI-AID KIT received FDA 510(k) clearance on 1996-11-12, under 510(k) number K963049.

Who is the listed applicant for STERI-AID KIT?

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

What is the FDA product code for STERI-AID KIT?

The FDA product code for STERI-AID KIT is FQZ.

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Related Devices (Code: FQZ)

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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