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FDA 510(k)

TIGER PATIENT EXAM GLOVES

K-Number: K892978 · 1989-08-29

ApplicantDaesung America Co., Inc.
Decision Date1989-08-29
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TIGER PATIENT EXAM GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Daesung America Co., Inc.. It received FDA 510(k) clearance on 1989-08-29 under 510(k) number K892978. 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 TIGER PATIENT EXAM GLOVES?

TIGER PATIENT EXAM GLOVES is a medical device that received FDA 510(k) clearance on 1989-08-29. The listed applicant is Daesung America Co., Inc.. The 510(k) number is K892978.

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

TIGER PATIENT EXAM GLOVES received FDA 510(k) clearance on 1989-08-29, under 510(k) number K892978.

Who is the listed applicant for TIGER PATIENT EXAM GLOVES?

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

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

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

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Official Source

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