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FDA 510(k)

DUBBLE BUTTERFLY PAT EXAM GLOVES/MFG: QUINGDAO FAC

K-Number: K893236 · 1989-08-15

Decision Date1989-08-15
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DUBBLE BUTTERFLY PAT EXAM GLOVES/MFG: QUINGDAO FAC 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 1989-08-15 under 510(k) number K893236. 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 DUBBLE BUTTERFLY PAT EXAM GLOVES/MFG: QUINGDAO FAC?

DUBBLE BUTTERFLY PAT EXAM GLOVES/MFG: QUINGDAO FAC is a medical device that received FDA 510(k) clearance on 1989-08-15. The listed applicant is China National Chemical Construction Corp.-Qingdao. The 510(k) number is K893236.

When did DUBBLE BUTTERFLY PAT EXAM GLOVES/MFG: QUINGDAO FAC receive FDA 510(k) clearance?

DUBBLE BUTTERFLY PAT EXAM GLOVES/MFG: QUINGDAO FAC received FDA 510(k) clearance on 1989-08-15, under 510(k) number K893236.

Who is the listed applicant for DUBBLE BUTTERFLY PAT EXAM GLOVES/MFG: QUINGDAO FAC?

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 DUBBLE BUTTERFLY PAT EXAM GLOVES/MFG: QUINGDAO FAC?

The FDA product code for DUBBLE BUTTERFLY PAT EXAM GLOVES/MFG: QUINGDAO FAC 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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