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FDA 510(k)

DERLIN

K-Number: K964817 · 1997-01-24

ApplicantDerlin Company , Ltd.
Decision Date1997-01-24
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DERLIN is the device name listed in this FDA 510(k) record. The listed applicant is Derlin Company , Ltd.. It received FDA 510(k) clearance on 1997-01-24 under 510(k) number K964817. 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 DERLIN?

DERLIN is a medical device that received FDA 510(k) clearance on 1997-01-24. The listed applicant is Derlin Company , Ltd.. The 510(k) number is K964817.

When did DERLIN receive FDA 510(k) clearance?

DERLIN received FDA 510(k) clearance on 1997-01-24, under 510(k) number K964817.

Who is the listed applicant for DERLIN?

The FDA 510(k) record lists Derlin Company , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DERLIN?

The FDA product code for DERLIN 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.

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Other records listing Derlin Company , 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.

K974223NITRILE, POWDER FREE, POLY COATED PATIENT EXAMINATION GLOVES

Related Devices (Code: LYY)

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Official Source

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