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FDA 510(k)

JOEY CLAMP OPENING TOOL

K-Number: K041332 · 2004-06-25

ApplicantMaternus, Inc.
Decision Date2004-06-25
Product CodeHFW
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

JOEY CLAMP OPENING TOOL is the device name listed in this FDA 510(k) record. The listed applicant is Maternus, Inc.. It received FDA 510(k) clearance on 2004-06-25 under 510(k) number K041332. 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 JOEY CLAMP OPENING TOOL?

JOEY CLAMP OPENING TOOL is a medical device that received FDA 510(k) clearance on 2004-06-25. The listed applicant is Maternus, Inc.. The 510(k) number is K041332.

When did JOEY CLAMP OPENING TOOL receive FDA 510(k) clearance?

JOEY CLAMP OPENING TOOL received FDA 510(k) clearance on 2004-06-25, under 510(k) number K041332.

Who is the listed applicant for JOEY CLAMP OPENING TOOL?

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

What is the FDA product code for JOEY CLAMP OPENING TOOL?

The FDA product code for JOEY CLAMP OPENING TOOL 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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Other records listing Maternus, 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.

K011621KOALA CLAMP, KOALA CLAMP AND CUTTERK010695KOALA CLAMP

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.

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.K010695KOALA CLAMPMaternus, 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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