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FDA 510(k)

PATIENT EXAM GLOVES (MFG. SUN FLOWER GLOVE CO.)

K-Number: K893072 · 1990-05-18

Decision Date1990-05-18
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT EXAM GLOVES (MFG. SUN FLOWER GLOVE CO.) is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Medical Suppliers. It received FDA 510(k) clearance on 1990-05-18 under 510(k) number K893072. The device is classified under product code LYZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATIENT EXAM GLOVES (MFG. SUN FLOWER GLOVE CO.)?

PATIENT EXAM GLOVES (MFG. SUN FLOWER GLOVE CO.) is a medical device that received FDA 510(k) clearance on 1990-05-18. The listed applicant is Innovative Medical Suppliers. The 510(k) number is K893072.

When did PATIENT EXAM GLOVES (MFG. SUN FLOWER GLOVE CO.) receive FDA 510(k) clearance?

PATIENT EXAM GLOVES (MFG. SUN FLOWER GLOVE CO.) received FDA 510(k) clearance on 1990-05-18, under 510(k) number K893072.

Who is the listed applicant for PATIENT EXAM GLOVES (MFG. SUN FLOWER GLOVE CO.)?

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

What is the FDA product code for PATIENT EXAM GLOVES (MFG. SUN FLOWER GLOVE CO.)?

The FDA product code for PATIENT EXAM GLOVES (MFG. SUN FLOWER GLOVE CO.) is LYZ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Innovative Medical Suppliers as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: LYZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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