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FDA 510(k)

THINKINGNET

K-Number: K010271 · 2001-04-03

Decision Date2001-04-03
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

THINKINGNET is the device name listed in this FDA 510(k) record. The listed applicant is Thinking Systems Corp.. It received FDA 510(k) clearance on 2001-04-03 under 510(k) number K010271. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THINKINGNET?

THINKINGNET is a medical device that received FDA 510(k) clearance on 2001-04-03. The listed applicant is Thinking Systems Corp.. The 510(k) number is K010271.

When did THINKINGNET receive FDA 510(k) clearance?

THINKINGNET received FDA 510(k) clearance on 2001-04-03, under 510(k) number K010271.

Who is the listed applicant for THINKINGNET?

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

What is the FDA product code for THINKINGNET?

The FDA product code for THINKINGNET is LLZ.

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 Thinking Systems 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: LLZ)

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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