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FDA 510(k)

MEDI, ULTRA, CURI EXAM GLOVES

K-Number: K893057 · 1989-07-28

ApplicantSinjaca Inc. Dba Sic Medical & Surgical Supplies
Decision Date1989-07-28
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDI, ULTRA, CURI EXAM GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Sinjaca Inc. Dba Sic Medical & Surgical Supplies. It received FDA 510(k) clearance on 1989-07-28 under 510(k) number K893057. 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, ULTRA, CURI EXAM GLOVES?

MEDI, ULTRA, CURI EXAM GLOVES is a medical device that received FDA 510(k) clearance on 1989-07-28. The listed applicant is Sinjaca Inc. Dba Sic Medical & Surgical Supplies. The 510(k) number is K893057.

When did MEDI, ULTRA, CURI EXAM GLOVES receive FDA 510(k) clearance?

MEDI, ULTRA, CURI EXAM GLOVES received FDA 510(k) clearance on 1989-07-28, under 510(k) number K893057.

Who is the listed applicant for MEDI, ULTRA, CURI EXAM GLOVES?

The FDA 510(k) record lists Sinjaca Inc. Dba Sic Medical & Surgical Supplies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDI, ULTRA, CURI EXAM GLOVES?

The FDA product code for MEDI, ULTRA, CURI EXAM GLOVES is LYY.

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Official Source

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