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FDA 510(k)

DESERET SURGEON'S GLOVE ACCESSORY

K-Number: K823086 · 1983-01-17

Decision Date1983-01-17
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DESERET SURGEON'S GLOVE ACCESSORY is the device name listed in this FDA 510(k) record. The listed applicant is Parke-Davis Co.. It received FDA 510(k) clearance on 1983-01-17 under 510(k) number K823086. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DESERET SURGEON'S GLOVE ACCESSORY?

DESERET SURGEON'S GLOVE ACCESSORY is a medical device that received FDA 510(k) clearance on 1983-01-17. The listed applicant is Parke-Davis Co.. The 510(k) number is K823086.

When did DESERET SURGEON'S GLOVE ACCESSORY receive FDA 510(k) clearance?

DESERET SURGEON'S GLOVE ACCESSORY received FDA 510(k) clearance on 1983-01-17, under 510(k) number K823086.

Who is the listed applicant for DESERET SURGEON'S GLOVE ACCESSORY?

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

What is the FDA product code for DESERET SURGEON'S GLOVE ACCESSORY?

The FDA product code for DESERET SURGEON'S GLOVE ACCESSORY is KGO.

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 Parke-Davis 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.

View all 47 devices →

Related Devices (Code: KGO)

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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