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FDA 510(k)

PATIENT EXAMINATION GLOVES (NON-STERILE VINYL)

K-Number: K890851 · 1989-04-25

Decision Date1989-04-25
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT EXAMINATION GLOVES (NON-STERILE VINYL) is the device name listed in this FDA 510(k) record. The listed applicant is Daw Shin Industrial Co., Ltd.. It received FDA 510(k) clearance on 1989-04-25 under 510(k) number K890851. 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 EXAMINATION GLOVES (NON-STERILE VINYL)?

PATIENT EXAMINATION GLOVES (NON-STERILE VINYL) is a medical device that received FDA 510(k) clearance on 1989-04-25. The listed applicant is Daw Shin Industrial Co., Ltd.. The 510(k) number is K890851.

When did PATIENT EXAMINATION GLOVES (NON-STERILE VINYL) receive FDA 510(k) clearance?

PATIENT EXAMINATION GLOVES (NON-STERILE VINYL) received FDA 510(k) clearance on 1989-04-25, under 510(k) number K890851.

Who is the listed applicant for PATIENT EXAMINATION GLOVES (NON-STERILE VINYL)?

The FDA 510(k) record lists Daw Shin Industrial Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PATIENT EXAMINATION GLOVES (NON-STERILE VINYL)?

The FDA product code for PATIENT EXAMINATION GLOVES (NON-STERILE VINYL) 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 Daw Shin Industrial Co., Ltd. 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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