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FDA 510(k)

NON-STERILE VINYL GLOVES

K-Number: K885346 · 1989-01-18

Decision Date1989-01-18
Product CodeFMC
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NON-STERILE VINYL GLOVES 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 1989-01-18 under 510(k) number K885346. The device is classified under product code FMC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NON-STERILE VINYL GLOVES?

NON-STERILE VINYL GLOVES is a medical device that received FDA 510(k) clearance on 1989-01-18. The listed applicant is Daw Shin Industrial Co., Ltd.. The 510(k) number is K885346.

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

NON-STERILE VINYL GLOVES received FDA 510(k) clearance on 1989-01-18, under 510(k) number K885346.

Who is the listed applicant for NON-STERILE VINYL GLOVES?

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 NON-STERILE VINYL GLOVES?

The FDA product code for NON-STERILE VINYL GLOVES is FMC.

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: FMC)

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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