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FDA 510(k)

SCAN COM AND SCAN COM P (TENTATIVE)

K-Number: K903652 · 1990-08-24

Decision Date1990-08-24
Product CodeILQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SCAN COM AND SCAN COM P (TENTATIVE) is the device name listed in this FDA 510(k) record. The listed applicant is Med Labs, Inc.. It received FDA 510(k) clearance on 1990-08-24 under 510(k) number K903652. The device is classified under product code ILQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCAN COM AND SCAN COM P (TENTATIVE)?

SCAN COM AND SCAN COM P (TENTATIVE) is a medical device that received FDA 510(k) clearance on 1990-08-24. The listed applicant is Med Labs, Inc.. The 510(k) number is K903652.

When did SCAN COM AND SCAN COM P (TENTATIVE) receive FDA 510(k) clearance?

SCAN COM AND SCAN COM P (TENTATIVE) received FDA 510(k) clearance on 1990-08-24, under 510(k) number K903652.

Who is the listed applicant for SCAN COM AND SCAN COM P (TENTATIVE)?

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

What is the FDA product code for SCAN COM AND SCAN COM P (TENTATIVE)?

The FDA product code for SCAN COM AND SCAN COM P (TENTATIVE) is ILQ.

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 Med Labs, 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.

Related Devices (Code: ILQ)

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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