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FDA 510(k)

SENSI TOUCH PATIENT EXAM GLOVES (VINYL)

K-Number: K892078 · 1990-01-11

Decision Date1990-01-11
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SENSI TOUCH PATIENT EXAM GLOVES (VINYL) is the device name listed in this FDA 510(k) record. The listed applicant is Taiwan Old Shop Corp.. It received FDA 510(k) clearance on 1990-01-11 under 510(k) number K892078. The device is classified under product code LYZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SENSI TOUCH PATIENT EXAM GLOVES (VINYL)?

SENSI TOUCH PATIENT EXAM GLOVES (VINYL) is a medical device that received FDA 510(k) clearance on 1990-01-11. The listed applicant is Taiwan Old Shop Corp.. The 510(k) number is K892078.

When did SENSI TOUCH PATIENT EXAM GLOVES (VINYL) receive FDA 510(k) clearance?

SENSI TOUCH PATIENT EXAM GLOVES (VINYL) received FDA 510(k) clearance on 1990-01-11, under 510(k) number K892078.

Who is the listed applicant for SENSI TOUCH PATIENT EXAM GLOVES (VINYL)?

The FDA 510(k) record lists Taiwan Old Shop Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SENSI TOUCH PATIENT EXAM GLOVES (VINYL)?

The FDA product code for SENSI TOUCH PATIENT EXAM GLOVES (VINYL) is LYZ.

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.

Related Devices (Code: LYZ)

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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