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FDA 510(k)

ANAGO ELECTRO SURGICAL TIP CLEANER

K-Number: K800058 · 1980-01-28

ApplicantAnago, Inc.
Decision Date1980-01-28
Product CodeGEC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ANAGO ELECTRO SURGICAL TIP CLEANER is the device name listed in this FDA 510(k) record. The listed applicant is Anago, Inc.. It received FDA 510(k) clearance on 1980-01-28 under 510(k) number K800058. The device is classified under product code GEC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANAGO ELECTRO SURGICAL TIP CLEANER?

ANAGO ELECTRO SURGICAL TIP CLEANER is a medical device that received FDA 510(k) clearance on 1980-01-28. The listed applicant is Anago, Inc.. The 510(k) number is K800058.

When did ANAGO ELECTRO SURGICAL TIP CLEANER receive FDA 510(k) clearance?

ANAGO ELECTRO SURGICAL TIP CLEANER received FDA 510(k) clearance on 1980-01-28, under 510(k) number K800058.

Who is the listed applicant for ANAGO ELECTRO SURGICAL TIP CLEANER?

The FDA 510(k) record lists Anago, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANAGO ELECTRO SURGICAL TIP CLEANER?

The FDA product code for ANAGO ELECTRO SURGICAL TIP CLEANER is GEC.

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 Anago, 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.

View all 44 devices →

Related Devices (Code: GEC)

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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