Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SCHULMAN DOUBLE UMBILICAL CORD CLAMP NO. 1000

K-Number: K863645 · 1986-09-25

ApplicantUnited Medical Systems, Inc.
Decision Date1986-09-25
Product CodeHFW
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SCHULMAN DOUBLE UMBILICAL CORD CLAMP NO. 1000 is the device name listed in this FDA 510(k) record. The listed applicant is United Medical Systems, Inc.. It received FDA 510(k) clearance on 1986-09-25 under 510(k) number K863645. 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 SCHULMAN DOUBLE UMBILICAL CORD CLAMP NO. 1000?

SCHULMAN DOUBLE UMBILICAL CORD CLAMP NO. 1000 is a medical device that received FDA 510(k) clearance on 1986-09-25. The listed applicant is United Medical Systems, Inc.. The 510(k) number is K863645.

When did SCHULMAN DOUBLE UMBILICAL CORD CLAMP NO. 1000 receive FDA 510(k) clearance?

SCHULMAN DOUBLE UMBILICAL CORD CLAMP NO. 1000 received FDA 510(k) clearance on 1986-09-25, under 510(k) number K863645.

Who is the listed applicant for SCHULMAN DOUBLE UMBILICAL CORD CLAMP NO. 1000?

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

What is the FDA product code for SCHULMAN DOUBLE UMBILICAL CORD CLAMP NO. 1000?

The FDA product code for SCHULMAN DOUBLE UMBILICAL CORD CLAMP NO. 1000 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing United Medical Systems, 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.

K072538PIEZOLITH 3000 TRIPLE-FOCUS LITHOTRIPTERK032958PIEZOLITH 3000 LITHOTRIPTER, MODEL 3000K894949SQAK893003TOCOLYTIC SITE CARE SUP KIT #1001/100A/CARRY CASE

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.

↑