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FDA 510(k)

BUSSE UMBILICAL CORD CLAMP CUTTER

K-Number: K021055 · 2002-04-29

ApplicantBusse Hospital Disposables, Inc.
Decision Date2002-04-29
Product CodeHFW
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

BUSSE UMBILICAL CORD CLAMP CUTTER is the device name listed in this FDA 510(k) record. The listed applicant is Busse Hospital Disposables, Inc.. It received FDA 510(k) clearance on 2002-04-29 under 510(k) number K021055. 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 BUSSE UMBILICAL CORD CLAMP CUTTER?

BUSSE UMBILICAL CORD CLAMP CUTTER is a medical device that received FDA 510(k) clearance on 2002-04-29. The listed applicant is Busse Hospital Disposables, Inc.. The 510(k) number is K021055.

When did BUSSE UMBILICAL CORD CLAMP CUTTER receive FDA 510(k) clearance?

BUSSE UMBILICAL CORD CLAMP CUTTER received FDA 510(k) clearance on 2002-04-29, under 510(k) number K021055.

Who is the listed applicant for BUSSE UMBILICAL CORD CLAMP CUTTER?

The FDA 510(k) record lists Busse Hospital Disposables, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BUSSE UMBILICAL CORD CLAMP CUTTER?

The FDA product code for BUSSE UMBILICAL CORD CLAMP CUTTER is HFW.

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Other records listing Busse Hospital Disposables, Inc. 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.

K120002I-STYLE BONE MARROW ASPIRATION NEEDLE WITH T-HANDLEK093909BUSSE SURGICAL DRAPES IVK092212BUSSE SURGICAL DRAPES IIIK082297BUSSE SURGICAL DRAPEK073222MODIFICATION TO:SPECIALTY NEEDLESK070465BUSSE EPIDURAL CATHETER

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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.K012917DYNAREX UMBILICAL CORD LAMP, MODELS 6833 AND 6833-BDynarex Corp.K011621KOALA CLAMP, KOALA CLAMP AND CUTTERMaternus, Inc.K010695KOALA CLAMPMaternus, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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