BOUIE ELECTROSURGICAL TIP CLEANER
K-Number: K802827 · 1980-12-11
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Device Summary
Frequently Asked Questions
What is the BOUIE ELECTROSURGICAL TIP CLEANER?
BOUIE ELECTROSURGICAL TIP CLEANER is a medical device that received FDA 510(k) clearance on 1980-12-11. The listed applicant is Sybron Corp.. The 510(k) number is K802827.
When did BOUIE ELECTROSURGICAL TIP CLEANER receive FDA 510(k) clearance?
BOUIE ELECTROSURGICAL TIP CLEANER received FDA 510(k) clearance on 1980-12-11, under 510(k) number K802827.
Who is the listed applicant for BOUIE ELECTROSURGICAL TIP CLEANER?
The FDA 510(k) record lists Sybron Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BOUIE ELECTROSURGICAL TIP CLEANER?
The FDA product code for BOUIE ELECTROSURGICAL TIP CLEANER is GEI.
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 Sybron Corp. 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: GEI)
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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