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FDA 510(k)

NOVA MICROSONICS CAPRICORN DIGITAL IMAGE SYSTEMS

K-Number: K905248 · 1991-02-28

Decision Date1991-02-28
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NOVA MICROSONICS CAPRICORN DIGITAL IMAGE SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Technology Laboratories, Inc.. It received FDA 510(k) clearance on 1991-02-28 under 510(k) number K905248. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOVA MICROSONICS CAPRICORN DIGITAL IMAGE SYSTEMS?

NOVA MICROSONICS CAPRICORN DIGITAL IMAGE SYSTEMS is a medical device that received FDA 510(k) clearance on 1991-02-28. The listed applicant is Advanced Technology Laboratories, Inc.. The 510(k) number is K905248.

When did NOVA MICROSONICS CAPRICORN DIGITAL IMAGE SYSTEMS receive FDA 510(k) clearance?

NOVA MICROSONICS CAPRICORN DIGITAL IMAGE SYSTEMS received FDA 510(k) clearance on 1991-02-28, under 510(k) number K905248.

Who is the listed applicant for NOVA MICROSONICS CAPRICORN DIGITAL IMAGE SYSTEMS?

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

What is the FDA product code for NOVA MICROSONICS CAPRICORN DIGITAL IMAGE SYSTEMS?

The FDA product code for NOVA MICROSONICS CAPRICORN DIGITAL IMAGE SYSTEMS is DQK.

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 Advanced Technology Laboratories, 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.

View all 61 devices →

Related Devices (Code: DQK)

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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