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FDA 510(k)

SUMMIT PATIENT EXAMINATION GLOVE

K-Number: K891171 · 1989-04-28

ApplicantTerng Nan Industrial Corp.
Decision Date1989-04-28
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SUMMIT PATIENT EXAMINATION GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Terng Nan Industrial Corp.. It received FDA 510(k) clearance on 1989-04-28 under 510(k) number K891171. 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 SUMMIT PATIENT EXAMINATION GLOVE?

SUMMIT PATIENT EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 1989-04-28. The listed applicant is Terng Nan Industrial Corp.. The 510(k) number is K891171.

When did SUMMIT PATIENT EXAMINATION GLOVE receive FDA 510(k) clearance?

SUMMIT PATIENT EXAMINATION GLOVE received FDA 510(k) clearance on 1989-04-28, under 510(k) number K891171.

Who is the listed applicant for SUMMIT PATIENT EXAMINATION GLOVE?

The FDA 510(k) record lists Terng Nan Industrial Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUMMIT PATIENT EXAMINATION GLOVE?

The FDA product code for SUMMIT PATIENT EXAMINATION GLOVE is LYY.

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Related Devices (Code: LYY)

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Official Source

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