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FDA 510(k)

CONTACT COMPOUNT SONOLAY. SAC-10A

K-Number: K771290 · 1977-08-03

Decision Date1977-08-03
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CONTACT COMPOUNT SONOLAY. SAC-10A is the device name listed in this FDA 510(k) record. The listed applicant is Toshiba Medical Systems. It received FDA 510(k) clearance on 1977-08-03 under 510(k) number K771290. 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 CONTACT COMPOUNT SONOLAY. SAC-10A?

CONTACT COMPOUNT SONOLAY. SAC-10A is a medical device that received FDA 510(k) clearance on 1977-08-03. The listed applicant is Toshiba Medical Systems. The 510(k) number is K771290.

When did CONTACT COMPOUNT SONOLAY. SAC-10A receive FDA 510(k) clearance?

CONTACT COMPOUNT SONOLAY. SAC-10A received FDA 510(k) clearance on 1977-08-03, under 510(k) number K771290.

Who is the listed applicant for CONTACT COMPOUNT SONOLAY. SAC-10A?

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

What is the FDA product code for CONTACT COMPOUNT SONOLAY. SAC-10A?

The FDA product code for CONTACT COMPOUNT SONOLAY. SAC-10A 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 Toshiba Medical Systems 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 54 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

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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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