OPERAND* ULTRASOUND TRANSMISSION GEL
K-Number: K951695 · 1995-05-12
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Device Summary
Frequently Asked Questions
What is the OPERAND* ULTRASOUND TRANSMISSION GEL?
OPERAND* ULTRASOUND TRANSMISSION GEL is a medical device that received FDA 510(k) clearance on 1995-05-12. The listed applicant is Redi Products, Inc.. The 510(k) number is K951695.
When did OPERAND* ULTRASOUND TRANSMISSION GEL receive FDA 510(k) clearance?
OPERAND* ULTRASOUND TRANSMISSION GEL received FDA 510(k) clearance on 1995-05-12, under 510(k) number K951695.
Who is the listed applicant for OPERAND* ULTRASOUND TRANSMISSION GEL?
The FDA 510(k) record lists Redi Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OPERAND* ULTRASOUND TRANSMISSION GEL?
The FDA product code for OPERAND* ULTRASOUND TRANSMISSION GEL is IYN.
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.
Related Devices (Code: IYN)
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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