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FDA 510(k)

SCANHEAD 2.25MHZ ADDED TO ULTRAMARK 8

K-Number: K843129 · 1984-12-06

Decision Date1984-12-06
Product CodeJOP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SCANHEAD 2.25MHZ ADDED TO ULTRAMARK 8 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 1984-12-06 under 510(k) number K843129. The device is classified under product code JOP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCANHEAD 2.25MHZ ADDED TO ULTRAMARK 8?

SCANHEAD 2.25MHZ ADDED TO ULTRAMARK 8 is a medical device that received FDA 510(k) clearance on 1984-12-06. The listed applicant is Advanced Technology Laboratories, Inc.. The 510(k) number is K843129.

When did SCANHEAD 2.25MHZ ADDED TO ULTRAMARK 8 receive FDA 510(k) clearance?

SCANHEAD 2.25MHZ ADDED TO ULTRAMARK 8 received FDA 510(k) clearance on 1984-12-06, under 510(k) number K843129.

Who is the listed applicant for SCANHEAD 2.25MHZ ADDED TO ULTRAMARK 8?

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 SCANHEAD 2.25MHZ ADDED TO ULTRAMARK 8?

The FDA product code for SCANHEAD 2.25MHZ ADDED TO ULTRAMARK 8 is JOP.

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.

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Related Devices (Code: JOP)

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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