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FDA 510(k)

ACCUTOUCH PATIENT EXAM GLOVES

K-Number: K892977 · 1989-08-01

ApplicantThai Medical Industries Co., Ltd.
Decision Date1989-08-01
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ACCUTOUCH PATIENT EXAM GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Thai Medical Industries Co., Ltd.. It received FDA 510(k) clearance on 1989-08-01 under 510(k) number K892977. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCUTOUCH PATIENT EXAM GLOVES?

ACCUTOUCH PATIENT EXAM GLOVES is a medical device that received FDA 510(k) clearance on 1989-08-01. The listed applicant is Thai Medical Industries Co., Ltd.. The 510(k) number is K892977.

When did ACCUTOUCH PATIENT EXAM GLOVES receive FDA 510(k) clearance?

ACCUTOUCH PATIENT EXAM GLOVES received FDA 510(k) clearance on 1989-08-01, under 510(k) number K892977.

Who is the listed applicant for ACCUTOUCH PATIENT EXAM GLOVES?

The FDA 510(k) record lists Thai Medical Industries Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACCUTOUCH PATIENT EXAM GLOVES?

The FDA product code for ACCUTOUCH PATIENT EXAM GLOVES is LYY.

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Related Devices (Code: LYY)

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Official Source

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