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FDA 510(k)

THREE GUN PATIENT EXAMINATION GLOVES

K-Number: K891951 · 1989-07-14

ApplicantBilwin Corp.
Decision Date1989-07-14
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

THREE GUN PATIENT EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Bilwin Corp.. It received FDA 510(k) clearance on 1989-07-14 under 510(k) number K891951. 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 THREE GUN PATIENT EXAMINATION GLOVES?

THREE GUN PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1989-07-14. The listed applicant is Bilwin Corp.. The 510(k) number is K891951.

When did THREE GUN PATIENT EXAMINATION GLOVES receive FDA 510(k) clearance?

THREE GUN PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 1989-07-14, under 510(k) number K891951.

Who is the listed applicant for THREE GUN PATIENT EXAMINATION GLOVES?

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

What is the FDA product code for THREE GUN PATIENT EXAMINATION GLOVES?

The FDA product code for THREE GUN PATIENT EXAMINATION GLOVES is LYY.

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Related Devices (Code: LYY)

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Official Source

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