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FDA 510(k)

SECURLINE UMBILICAL CORD CLAMP #3505 STERILE #3515 NON-STERILE

K-Number: K020718 · 2002-06-03

ApplicantPrecision Dynamics Corp.
Decision Date2002-06-03
Product CodeHFW
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SECURLINE UMBILICAL CORD CLAMP #3505 STERILE #3515 NON-STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Precision Dynamics Corp.. It received FDA 510(k) clearance on 2002-06-03 under 510(k) number K020718. 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 SECURLINE UMBILICAL CORD CLAMP #3505 STERILE #3515 NON-STERILE?

SECURLINE UMBILICAL CORD CLAMP #3505 STERILE #3515 NON-STERILE is a medical device that received FDA 510(k) clearance on 2002-06-03. The listed applicant is Precision Dynamics Corp.. The 510(k) number is K020718.

When did SECURLINE UMBILICAL CORD CLAMP #3505 STERILE #3515 NON-STERILE receive FDA 510(k) clearance?

SECURLINE UMBILICAL CORD CLAMP #3505 STERILE #3515 NON-STERILE received FDA 510(k) clearance on 2002-06-03, under 510(k) number K020718.

Who is the listed applicant for SECURLINE UMBILICAL CORD CLAMP #3505 STERILE #3515 NON-STERILE?

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

What is the FDA product code for SECURLINE UMBILICAL CORD CLAMP #3505 STERILE #3515 NON-STERILE?

The FDA product code for SECURLINE UMBILICAL CORD CLAMP #3505 STERILE #3515 NON-STERILE is HFW.

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Other records listing Precision Dynamics Corp. 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.

K994353SECURELINE DISPOSABLE FETAL MONITORING STRAPS #3860 AND #3565K994263SECURLINE UMBILICAL CORD CLAMP CLIPPER #3540K990737'ECURLINE UMBILICAL CORD CLAMP #3500K884357PRECISION BIOPORT COLLECTION & TRANSPORT SYSTEMK882580MECHANICAL CHANGE IN IN-VITRO MICRO DEVICEK874665SECURLINE FINE NEEDLE ASPIRATION BIOPSY TRAY

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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.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

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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