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FDA 510(k)

POWDER FREE TACTYLON SURGEONS GLOVE

K-Number: K955419 · 1996-04-15

Decision Date1996-04-15
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

POWDER FREE TACTYLON SURGEONS GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Tactyl Technologies, Inc.. It received FDA 510(k) clearance on 1996-04-15 under 510(k) number K955419. 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 POWDER FREE TACTYLON SURGEONS GLOVE?

POWDER FREE TACTYLON SURGEONS GLOVE is a medical device that received FDA 510(k) clearance on 1996-04-15. The listed applicant is Tactyl Technologies, Inc.. The 510(k) number is K955419.

When did POWDER FREE TACTYLON SURGEONS GLOVE receive FDA 510(k) clearance?

POWDER FREE TACTYLON SURGEONS GLOVE received FDA 510(k) clearance on 1996-04-15, under 510(k) number K955419.

Who is the listed applicant for POWDER FREE TACTYLON SURGEONS GLOVE?

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

What is the FDA product code for POWDER FREE TACTYLON SURGEONS GLOVE?

The FDA product code for POWDER FREE TACTYLON SURGEONS 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 Tactyl Technologies, 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 7 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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