FDA 510(k)

FH LEN

K-Number: K872503 · 1987-07-27

ApplicantFu Heng First Industrial Co., Ltd.

Decision Date1987-07-27

Product CodeHQY

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

FH LEN is the device name listed in this FDA 510(k) record. The listed applicant is Fu Heng First Industrial Co., Ltd.. It received FDA 510(k) clearance on 1987-07-27 under 510(k) number K872503. The device is classified under product code HQY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FH LEN?

FH LEN is a medical device that received FDA 510(k) clearance on 1987-07-27. The listed applicant is Fu Heng First Industrial Co., Ltd.. The 510(k) number is K872503.

When did FH LEN receive FDA 510(k) clearance?

FH LEN received FDA 510(k) clearance on 1987-07-27, under 510(k) number K872503.

Who is the listed applicant for FH LEN?

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

What is the FDA product code for FH LEN?

The FDA product code for FH LEN is HQY.

Related Devices (Code: HQY)

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.

K974852NON-PRESCRIPTION SUNGLASSESChia Hui Spectacles Mfg. Corp.K974860NON-PRESCRIPTION SUNGLASSESWenzhou Ming Ming Optical Co. , Ltd.K974861NON-PRESCRIPTION SUNGLASSESWenzhou Hindar Optical Co., Ltd.K974511SUNGLASSESSun World Intl., Inc.K974441SUNGLASSESHip Shing Fat Co., Ltd.K973528SUNGLASSESJeou Jeou Long Industrial Co., Ltd.

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.