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FDA 510(k)

THE DENVER CAUTERY

K-Number: K922062 · 1993-01-12

ApplicantDenver Splint Co.
Decision Date1993-01-12
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

THE DENVER CAUTERY is the device name listed in this FDA 510(k) record. The listed applicant is Denver Splint Co.. It received FDA 510(k) clearance on 1993-01-12 under 510(k) number K922062. 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 THE DENVER CAUTERY?

THE DENVER CAUTERY is a medical device that received FDA 510(k) clearance on 1993-01-12. The listed applicant is Denver Splint Co.. The 510(k) number is K922062.

When did THE DENVER CAUTERY receive FDA 510(k) clearance?

THE DENVER CAUTERY received FDA 510(k) clearance on 1993-01-12, under 510(k) number K922062.

Who is the listed applicant for THE DENVER CAUTERY?

The FDA 510(k) record lists Denver Splint Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE DENVER CAUTERY?

The FDA product code for THE DENVER CAUTERY 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.

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Other records listing Denver Splint Co. 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.

K940798SHIPPERT PRESSURE BANDAGEK940133THE EXPANDACELL EAR PACKK935724THE EXPANDACELL SINUS PACK

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.

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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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