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FDA 510(k)

THIELER KIT

K-Number: K875153 · 1988-02-18

ApplicantTaris Corp.
Decision Date1988-02-18
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

THIELER KIT is the device name listed in this FDA 510(k) record. The listed applicant is Taris Corp.. It received FDA 510(k) clearance on 1988-02-18 under 510(k) number K875153. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THIELER KIT?

THIELER KIT is a medical device that received FDA 510(k) clearance on 1988-02-18. The listed applicant is Taris Corp.. The 510(k) number is K875153.

When did THIELER KIT receive FDA 510(k) clearance?

THIELER KIT received FDA 510(k) clearance on 1988-02-18, under 510(k) number K875153.

Who is the listed applicant for THIELER KIT?

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

What is the FDA product code for THIELER KIT?

The FDA product code for THIELER KIT is KKX.

Related Clinical Trials

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.

Other records listing Taris Corp. 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.

Related Devices (Code: KKX)

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.

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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