FDA 510(k)

EZ-CIRC

K-Number: K963223 · 1997-04-23

Decision Date1997-04-23

Product CodeHFW

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

EZ-CIRC is the device name listed in this FDA 510(k) record. The listed applicant is Phyllis Adams, Rn, Npc, Msn. It received FDA 510(k) clearance on 1997-04-23 under 510(k) number K963223. 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 EZ-CIRC?

EZ-CIRC is a medical device that received FDA 510(k) clearance on 1997-04-23. The listed applicant is Phyllis Adams, Rn, Npc, Msn. The 510(k) number is K963223.

When did EZ-CIRC receive FDA 510(k) clearance?

EZ-CIRC received FDA 510(k) clearance on 1997-04-23, under 510(k) number K963223.

Who is the listed applicant for EZ-CIRC?

The FDA 510(k) record lists Phyllis Adams, Rn, Npc, Msn as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EZ-CIRC?

The FDA product code for EZ-CIRC is HFW.

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.