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FDA 510(k)

THE KEYMED SIGMOIDOSCOPE DISINFECTION STAND

K-Number: K860704 · 1986-06-17

ApplicantKeymed, Inc.
Decision Date1986-06-17
Product CodeNZA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

THE KEYMED SIGMOIDOSCOPE DISINFECTION STAND is the device name listed in this FDA 510(k) record. The listed applicant is Keymed, Inc.. It received FDA 510(k) clearance on 1986-06-17 under 510(k) number K860704. The device is classified under product code NZA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE KEYMED SIGMOIDOSCOPE DISINFECTION STAND?

THE KEYMED SIGMOIDOSCOPE DISINFECTION STAND is a medical device that received FDA 510(k) clearance on 1986-06-17. The listed applicant is Keymed, Inc.. The 510(k) number is K860704.

When did THE KEYMED SIGMOIDOSCOPE DISINFECTION STAND receive FDA 510(k) clearance?

THE KEYMED SIGMOIDOSCOPE DISINFECTION STAND received FDA 510(k) clearance on 1986-06-17, under 510(k) number K860704.

Who is the listed applicant for THE KEYMED SIGMOIDOSCOPE DISINFECTION STAND?

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

What is the FDA product code for THE KEYMED SIGMOIDOSCOPE DISINFECTION STAND?

The FDA product code for THE KEYMED SIGMOIDOSCOPE DISINFECTION STAND is NZA.

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 Keymed, 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.

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Related Devices (Code: NZA)

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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