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FDA 510(k)

QFC UMBILICAL CLAMP

K-Number: K963889 · 1997-04-18

ApplicantQfc Industries
Decision Date1997-04-18
Product CodeHFW
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

QFC UMBILICAL CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Qfc Industries. It received FDA 510(k) clearance on 1997-04-18 under 510(k) number K963889. The device is classified under product code HFW. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QFC UMBILICAL CLAMP?

QFC UMBILICAL CLAMP is a medical device that received FDA 510(k) clearance on 1997-04-18. The listed applicant is Qfc Industries. The 510(k) number is K963889.

When did QFC UMBILICAL CLAMP receive FDA 510(k) clearance?

QFC UMBILICAL CLAMP received FDA 510(k) clearance on 1997-04-18, under 510(k) number K963889.

Who is the listed applicant for QFC UMBILICAL CLAMP?

The FDA 510(k) record lists Qfc Industries as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QFC UMBILICAL CLAMP?

The FDA product code for QFC UMBILICAL CLAMP is HFW.

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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Related Devices (Code: HFW)

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.

K041332JOEY CLAMP OPENING TOOLMaternus, Inc.K033846KAEN YIH UMBILICAL CORD CLAMPKaen Yih Enterprise Co., Ltd.K020718SECURLINE UMBILICAL CORD CLAMP #3505 STERILE #3515 NON-STERILEPrecision Dynamics Corp.K021055BUSSE UMBILICAL CORD CLAMP CUTTERBusse Hospital Disposables, Inc.K012917DYNAREX UMBILICAL CORD LAMP, MODELS 6833 AND 6833-BDynarex Corp.K011621KOALA CLAMP, KOALA CLAMP AND CUTTERMaternus, Inc.

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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