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FDA 510(k)

SMV 120 SONIC MAMMOGRAPHIC VIEWER

K-Number: K792585 · 1980-01-21

Decision Date1980-01-21
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SMV 120 SONIC MAMMOGRAPHIC VIEWER is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1980-01-21 under 510(k) number K792585. 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 SMV 120 SONIC MAMMOGRAPHIC VIEWER?

SMV 120 SONIC MAMMOGRAPHIC VIEWER is a medical device that received FDA 510(k) clearance on 1980-01-21. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K792585.

When did SMV 120 SONIC MAMMOGRAPHIC VIEWER receive FDA 510(k) clearance?

SMV 120 SONIC MAMMOGRAPHIC VIEWER received FDA 510(k) clearance on 1980-01-21, under 510(k) number K792585.

Who is the listed applicant for SMV 120 SONIC MAMMOGRAPHIC VIEWER?

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

What is the FDA product code for SMV 120 SONIC MAMMOGRAPHIC VIEWER?

The FDA product code for SMV 120 SONIC MAMMOGRAPHIC VIEWER 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 Johnson & Johnson Professionals, 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 206 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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