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FDA 510(k)

MEDI + FORM EXAM (MFG: GLOVE SEAL SDN BHD)

K-Number: K893719 · 1989-09-13

ApplicantWorld Impex Corp.
Decision Date1989-09-13
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDI + FORM EXAM (MFG: GLOVE SEAL SDN BHD) is the device name listed in this FDA 510(k) record. The listed applicant is World Impex Corp.. It received FDA 510(k) clearance on 1989-09-13 under 510(k) number K893719. 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 MEDI + FORM EXAM (MFG: GLOVE SEAL SDN BHD)?

MEDI + FORM EXAM (MFG: GLOVE SEAL SDN BHD) is a medical device that received FDA 510(k) clearance on 1989-09-13. The listed applicant is World Impex Corp.. The 510(k) number is K893719.

When did MEDI + FORM EXAM (MFG: GLOVE SEAL SDN BHD) receive FDA 510(k) clearance?

MEDI + FORM EXAM (MFG: GLOVE SEAL SDN BHD) received FDA 510(k) clearance on 1989-09-13, under 510(k) number K893719.

Who is the listed applicant for MEDI + FORM EXAM (MFG: GLOVE SEAL SDN BHD)?

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

What is the FDA product code for MEDI + FORM EXAM (MFG: GLOVE SEAL SDN BHD)?

The FDA product code for MEDI + FORM EXAM (MFG: GLOVE SEAL SDN BHD) is LYY.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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