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FDA 510(k)

SONAR-AID(R) ULTRASOUND STANDOFF PAD

K-Number: K874943 · 1988-07-25

ApplicantGeistlich-Pharma
Decision Date1988-07-25
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SONAR-AID(R) ULTRASOUND STANDOFF PAD is the device name listed in this FDA 510(k) record. The listed applicant is Geistlich-Pharma. It received FDA 510(k) clearance on 1988-07-25 under 510(k) number K874943. 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 SONAR-AID(R) ULTRASOUND STANDOFF PAD?

SONAR-AID(R) ULTRASOUND STANDOFF PAD is a medical device that received FDA 510(k) clearance on 1988-07-25. The listed applicant is Geistlich-Pharma. The 510(k) number is K874943.

When did SONAR-AID(R) ULTRASOUND STANDOFF PAD receive FDA 510(k) clearance?

SONAR-AID(R) ULTRASOUND STANDOFF PAD received FDA 510(k) clearance on 1988-07-25, under 510(k) number K874943.

Who is the listed applicant for SONAR-AID(R) ULTRASOUND STANDOFF PAD?

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

What is the FDA product code for SONAR-AID(R) ULTRASOUND STANDOFF PAD?

The FDA product code for SONAR-AID(R) ULTRASOUND STANDOFF PAD is ITX.

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Related Devices (Code: ITX)

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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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