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FDA 510(k)

QUANTIMAP III

K-Number: K863650 · 1986-09-26

ApplicantQuantified Signal Imaging, Inc.
Decision Date1986-09-26
Product CodeOLT
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

QUANTIMAP III is the device name listed in this FDA 510(k) record. The listed applicant is Quantified Signal Imaging, Inc.. It received FDA 510(k) clearance on 1986-09-26 under 510(k) number K863650. The device is classified under product code OLT. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUANTIMAP III?

QUANTIMAP III is a medical device that received FDA 510(k) clearance on 1986-09-26. The listed applicant is Quantified Signal Imaging, Inc.. The 510(k) number is K863650.

When did QUANTIMAP III receive FDA 510(k) clearance?

QUANTIMAP III received FDA 510(k) clearance on 1986-09-26, under 510(k) number K863650.

Who is the listed applicant for QUANTIMAP III?

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

What is the FDA product code for QUANTIMAP III?

The FDA product code for QUANTIMAP III is OLT.

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.

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Other records listing Quantified Signal Imaging, 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.

K904294QSI 9500K894560QSI 9000

Related Devices (Code: OLT)

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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