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FDA 510(k)

AMEDA/EGNELL DOLPHIN UMBILICAL CORD SEVERING DEVIC

K-Number: K901954 · 1990-07-26

ApplicantHollister, Inc.
Decision Date1990-07-26
Product CodeHFW
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

AMEDA/EGNELL DOLPHIN UMBILICAL CORD SEVERING DEVIC is the device name listed in this FDA 510(k) record. The listed applicant is Hollister, Inc.. It received FDA 510(k) clearance on 1990-07-26 under 510(k) number K901954. 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 AMEDA/EGNELL DOLPHIN UMBILICAL CORD SEVERING DEVIC?

AMEDA/EGNELL DOLPHIN UMBILICAL CORD SEVERING DEVIC is a medical device that received FDA 510(k) clearance on 1990-07-26. The listed applicant is Hollister, Inc.. The 510(k) number is K901954.

When did AMEDA/EGNELL DOLPHIN UMBILICAL CORD SEVERING DEVIC receive FDA 510(k) clearance?

AMEDA/EGNELL DOLPHIN UMBILICAL CORD SEVERING DEVIC received FDA 510(k) clearance on 1990-07-26, under 510(k) number K901954.

Who is the listed applicant for AMEDA/EGNELL DOLPHIN UMBILICAL CORD SEVERING DEVIC?

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

What is the FDA product code for AMEDA/EGNELL DOLPHIN UMBILICAL CORD SEVERING DEVIC?

The FDA product code for AMEDA/EGNELL DOLPHIN UMBILICAL CORD SEVERING DEVIC is HFW.

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Other records listing Hollister, Inc. as applicant

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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

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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