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FDA 510(k)

ASLI

K-Number: K973473 · 1997-09-26

ApplicantTexin Industrial (International) , Ltd.
Decision Date1997-09-26
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ASLI is the device name listed in this FDA 510(k) record. The listed applicant is Texin Industrial (International) , Ltd.. It received FDA 510(k) clearance on 1997-09-26 under 510(k) number K973473. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASLI?

ASLI is a medical device that received FDA 510(k) clearance on 1997-09-26. The listed applicant is Texin Industrial (International) , Ltd.. The 510(k) number is K973473.

When did ASLI receive FDA 510(k) clearance?

ASLI received FDA 510(k) clearance on 1997-09-26, under 510(k) number K973473.

Who is the listed applicant for ASLI?

The FDA 510(k) record lists Texin Industrial (International) , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ASLI?

The FDA product code for ASLI is IOR.

Related Devices (Code: IOR)

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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