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FDA 510(k)

RAPID-AID THERAPEUTIC/SCANNING ULTRASOUND GEL

K-Number: K963169 · 1996-11-12

ApplicantRapid-Aid Ltd./Ltee
Decision Date1996-11-12
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RAPID-AID THERAPEUTIC/SCANNING ULTRASOUND GEL is the device name listed in this FDA 510(k) record. The listed applicant is Rapid-Aid Ltd./Ltee. It received FDA 510(k) clearance on 1996-11-12 under 510(k) number K963169. 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 RAPID-AID THERAPEUTIC/SCANNING ULTRASOUND GEL?

RAPID-AID THERAPEUTIC/SCANNING ULTRASOUND GEL is a medical device that received FDA 510(k) clearance on 1996-11-12. The listed applicant is Rapid-Aid Ltd./Ltee. The 510(k) number is K963169.

When did RAPID-AID THERAPEUTIC/SCANNING ULTRASOUND GEL receive FDA 510(k) clearance?

RAPID-AID THERAPEUTIC/SCANNING ULTRASOUND GEL received FDA 510(k) clearance on 1996-11-12, under 510(k) number K963169.

Who is the listed applicant for RAPID-AID THERAPEUTIC/SCANNING ULTRASOUND GEL?

The FDA 510(k) record lists Rapid-Aid Ltd./Ltee as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RAPID-AID THERAPEUTIC/SCANNING ULTRASOUND GEL?

The FDA product code for RAPID-AID THERAPEUTIC/SCANNING ULTRASOUND GEL 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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