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FDA 510(k)

BOUIE ELECTROSURGICAL TIP CLEANER

K-Number: K802827 · 1980-12-11

ApplicantSybron Corp.
Decision Date1980-12-11
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BOUIE ELECTROSURGICAL TIP CLEANER is the device name listed in this FDA 510(k) record. The listed applicant is Sybron Corp.. It received FDA 510(k) clearance on 1980-12-11 under 510(k) number K802827. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 37 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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