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)

TEMPORARY HEMO CLIP, 07-096-01/02 & APPLY FORCEP

K-Number: K862696 · 1986-07-30

ApplicantDowns Surgical , Ltd.
Decision Date1986-07-30
Product CodeHBT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TEMPORARY HEMO CLIP, 07-096-01/02 & APPLY FORCEP is the device name listed in this FDA 510(k) record. The listed applicant is Downs Surgical , Ltd.. It received FDA 510(k) clearance on 1986-07-30 under 510(k) number K862696. The device is classified under product code HBT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEMPORARY HEMO CLIP, 07-096-01/02 & APPLY FORCEP?

TEMPORARY HEMO CLIP, 07-096-01/02 & APPLY FORCEP is a medical device that received FDA 510(k) clearance on 1986-07-30. The listed applicant is Downs Surgical , Ltd.. The 510(k) number is K862696.

When did TEMPORARY HEMO CLIP, 07-096-01/02 & APPLY FORCEP receive FDA 510(k) clearance?

TEMPORARY HEMO CLIP, 07-096-01/02 & APPLY FORCEP received FDA 510(k) clearance on 1986-07-30, under 510(k) number K862696.

Who is the listed applicant for TEMPORARY HEMO CLIP, 07-096-01/02 & APPLY FORCEP?

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

What is the FDA product code for TEMPORARY HEMO CLIP, 07-096-01/02 & APPLY FORCEP?

The FDA product code for TEMPORARY HEMO CLIP, 07-096-01/02 & APPLY FORCEP is HBT.

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 Downs Surgical , Ltd. 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.

K903750ISLAM STERNAL PUNCTURE NEEDLE, CAT #AG-598-OO-EK903747ISLAM STERNAL PUNCTURE NEEDLE, CAT # AG-592-00-UK903749ISLAM STERNAL PUNCTURE NEEDLE, CAT #AG-596-00-UK903748ISLAM STERNAL PUNCTURE NEEDLE, CAT # AF-594-00-VK900609SHEPPERD STRAIGHT AND CURVED NEEDLESK900616SHEPPERD CUTTING FORCEPS

View all 60 devices →

Related Devices (Code: HBT)

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.

K924929REFLEX(R) ECARichard-Allan MedicalK896262TITANIUM LIGATING CLIPSRichard-Allan Medical Ind., Inc.K800318DOUBLETIME 2-TIPPED APPLIERS FOR HEMOCLIEdward Weck, 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.

↑