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FDA 510(k)

SONOLAYER-L, SAL-77A

K-Number: K852090 · 1985-12-02

Decision Date1985-12-02
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SONOLAYER-L, SAL-77A 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 1985-12-02 under 510(k) number K852090. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONOLAYER-L, SAL-77A?

SONOLAYER-L, SAL-77A is a medical device that received FDA 510(k) clearance on 1985-12-02. The listed applicant is Toshiba Medical Systems. The 510(k) number is K852090.

When did SONOLAYER-L, SAL-77A receive FDA 510(k) clearance?

SONOLAYER-L, SAL-77A received FDA 510(k) clearance on 1985-12-02, under 510(k) number K852090.

Who is the listed applicant for SONOLAYER-L, SAL-77A?

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 SONOLAYER-L, SAL-77A?

The FDA product code for SONOLAYER-L, SAL-77A is ITX.

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: ITX)

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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