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FDA 510(k)

SUMMA PROTECH: DELTA SERIES PATIENT EXAM GLOVES

K-Number: K891879 · 1989-06-06

ApplicantSumma Intl.
Decision Date1989-06-06
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SUMMA PROTECH: DELTA SERIES PATIENT EXAM GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Summa Intl.. It received FDA 510(k) clearance on 1989-06-06 under 510(k) number K891879. 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 SUMMA PROTECH: DELTA SERIES PATIENT EXAM GLOVES?

SUMMA PROTECH: DELTA SERIES PATIENT EXAM GLOVES is a medical device that received FDA 510(k) clearance on 1989-06-06. The listed applicant is Summa Intl.. The 510(k) number is K891879.

When did SUMMA PROTECH: DELTA SERIES PATIENT EXAM GLOVES receive FDA 510(k) clearance?

SUMMA PROTECH: DELTA SERIES PATIENT EXAM GLOVES received FDA 510(k) clearance on 1989-06-06, under 510(k) number K891879.

Who is the listed applicant for SUMMA PROTECH: DELTA SERIES PATIENT EXAM GLOVES?

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

What is the FDA product code for SUMMA PROTECH: DELTA SERIES PATIENT EXAM GLOVES?

The FDA product code for SUMMA PROTECH: DELTA SERIES PATIENT EXAM GLOVES is LYY.

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Related Devices (Code: LYY)

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Official Source

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