ULTRA-WET
K-Number: K820216 · 1982-02-24
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Device Summary
Frequently Asked Questions
What is the ULTRA-WET?
ULTRA-WET is a medical device that received FDA 510(k) clearance on 1982-02-24. The listed applicant is Buffalo Dental Mfg. Co., Inc.. The 510(k) number is K820216.
When did ULTRA-WET receive FDA 510(k) clearance?
ULTRA-WET received FDA 510(k) clearance on 1982-02-24, under 510(k) number K820216.
Who is the listed applicant for ULTRA-WET?
The FDA 510(k) record lists Buffalo Dental Mfg. Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ULTRA-WET?
The FDA product code for ULTRA-WET is ELW.
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 Buffalo Dental Mfg. Co., Inc. 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: ELW)
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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