FDA 510(k)

KBTC

K-Number: K950720 · 1995-03-01

Decision Date1995-03-01

Product CodeHQY

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

KBTC is the device name listed in this FDA 510(k) record. The listed applicant is Kyong-Buk Trading Corp.. It received FDA 510(k) clearance on 1995-03-01 under 510(k) number K950720. 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 KBTC?

KBTC is a medical device that received FDA 510(k) clearance on 1995-03-01. The listed applicant is Kyong-Buk Trading Corp.. The 510(k) number is K950720.

When did KBTC receive FDA 510(k) clearance?

KBTC received FDA 510(k) clearance on 1995-03-01, under 510(k) number K950720.

Who is the listed applicant for KBTC?

The FDA 510(k) record lists Kyong-Buk Trading Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KBTC?

The FDA product code for KBTC 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.