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FDA 510(k)

ADR REAL-TIME SECTOR SCANNER

K-Number: K792446 · 1980-01-09

Decision Date1980-01-09
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ADR REAL-TIME SECTOR SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is Adr Ultrasound. It received FDA 510(k) clearance on 1980-01-09 under 510(k) number K792446. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADR REAL-TIME SECTOR SCANNER?

ADR REAL-TIME SECTOR SCANNER is a medical device that received FDA 510(k) clearance on 1980-01-09. The listed applicant is Adr Ultrasound. The 510(k) number is K792446.

When did ADR REAL-TIME SECTOR SCANNER receive FDA 510(k) clearance?

ADR REAL-TIME SECTOR SCANNER received FDA 510(k) clearance on 1980-01-09, under 510(k) number K792446.

Who is the listed applicant for ADR REAL-TIME SECTOR SCANNER?

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

What is the FDA product code for ADR REAL-TIME SECTOR SCANNER?

The FDA product code for ADR REAL-TIME SECTOR SCANNER is IYO.

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 Adr Ultrasound 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 10 devices →

Related Devices (Code: IYO)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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