KITECKO ULTRASOUND STANDOFF PAD
K-Number: K851982 · 1985-08-14
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Device Summary
Frequently Asked Questions
What is the KITECKO ULTRASOUND STANDOFF PAD?
KITECKO ULTRASOUND STANDOFF PAD is a medical device that received FDA 510(k) clearance on 1985-08-14. The listed applicant is 3M Company. The 510(k) number is K851982.
When did KITECKO ULTRASOUND STANDOFF PAD receive FDA 510(k) clearance?
KITECKO ULTRASOUND STANDOFF PAD received FDA 510(k) clearance on 1985-08-14, under 510(k) number K851982.
Who is the listed applicant for KITECKO ULTRASOUND STANDOFF PAD?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KITECKO ULTRASOUND STANDOFF PAD?
The FDA product code for KITECKO ULTRASOUND STANDOFF PAD 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 3M Company 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.
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
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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