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FDA 510(k)

SURGIKOS NEUTRALON BR. SURGEON'S GLOVE

K-Number: K800152 · 1980-02-19

Decision Date1980-02-19
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGIKOS NEUTRALON BR. SURGEON'S GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Surgikos, Inc.. It received FDA 510(k) clearance on 1980-02-19 under 510(k) number K800152. 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 SURGIKOS NEUTRALON BR. SURGEON'S GLOVE?

SURGIKOS NEUTRALON BR. SURGEON'S GLOVE is a medical device that received FDA 510(k) clearance on 1980-02-19. The listed applicant is Surgikos, Inc.. The 510(k) number is K800152.

When did SURGIKOS NEUTRALON BR. SURGEON'S GLOVE receive FDA 510(k) clearance?

SURGIKOS NEUTRALON BR. SURGEON'S GLOVE received FDA 510(k) clearance on 1980-02-19, under 510(k) number K800152.

Who is the listed applicant for SURGIKOS NEUTRALON BR. SURGEON'S GLOVE?

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

What is the FDA product code for SURGIKOS NEUTRALON BR. SURGEON'S GLOVE?

The FDA product code for SURGIKOS NEUTRALON BR. SURGEON'S GLOVE 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 Surgikos, 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 56 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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