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FDA 510(k)

PATIENT EXAMINATION GLOVES DUBBLE BUTTERFLY

K-Number: K892685 · 1989-08-10

Decision Date1989-08-10
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT EXAMINATION GLOVES DUBBLE BUTTERFLY is the device name listed in this FDA 510(k) record. The listed applicant is China National Chemical Construction Corp.-Qingdao. It received FDA 510(k) clearance on 1989-08-10 under 510(k) number K892685. 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 PATIENT EXAMINATION GLOVES DUBBLE BUTTERFLY?

PATIENT EXAMINATION GLOVES DUBBLE BUTTERFLY is a medical device that received FDA 510(k) clearance on 1989-08-10. The listed applicant is China National Chemical Construction Corp.-Qingdao. The 510(k) number is K892685.

When did PATIENT EXAMINATION GLOVES DUBBLE BUTTERFLY receive FDA 510(k) clearance?

PATIENT EXAMINATION GLOVES DUBBLE BUTTERFLY received FDA 510(k) clearance on 1989-08-10, under 510(k) number K892685.

Who is the listed applicant for PATIENT EXAMINATION GLOVES DUBBLE BUTTERFLY?

The FDA 510(k) record lists China National Chemical Construction Corp.-Qingdao as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PATIENT EXAMINATION GLOVES DUBBLE BUTTERFLY?

The FDA product code for PATIENT EXAMINATION GLOVES DUBBLE BUTTERFLY is LYY.

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 China National Chemical Construction Corp.-Qingdao 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: LYY)

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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