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FDA 510(k)

BUTTERFLY GLOBE (PATIENT EXAMINATION GLOVE)

K-Number: K890982 · 1989-04-04

ApplicantO.L. Trading, Inc.
Decision Date1989-04-04
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BUTTERFLY GLOBE (PATIENT EXAMINATION GLOVE) is the device name listed in this FDA 510(k) record. The listed applicant is O.L. Trading, Inc.. It received FDA 510(k) clearance on 1989-04-04 under 510(k) number K890982. 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 BUTTERFLY GLOBE (PATIENT EXAMINATION GLOVE)?

BUTTERFLY GLOBE (PATIENT EXAMINATION GLOVE) is a medical device that received FDA 510(k) clearance on 1989-04-04. The listed applicant is O.L. Trading, Inc.. The 510(k) number is K890982.

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

BUTTERFLY GLOBE (PATIENT EXAMINATION GLOVE) received FDA 510(k) clearance on 1989-04-04, under 510(k) number K890982.

Who is the listed applicant for BUTTERFLY GLOBE (PATIENT EXAMINATION GLOVE)?

The FDA 510(k) record lists O.L. Trading, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BUTTERFLY GLOBE (PATIENT EXAMINATION GLOVE)?

The FDA product code for BUTTERFLY GLOBE (PATIENT EXAMINATION GLOVE) is LYY.

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Official Source

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