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)

SECU-TAPE UNIVERSAL FLEXIBLE MEDICAL CLAMPS

K-Number: K850503 · 1985-04-01

ApplicantTurn Needle Intl., Inc.
Decision Date1985-04-01
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SECU-TAPE UNIVERSAL FLEXIBLE MEDICAL CLAMPS is the device name listed in this FDA 510(k) record. The listed applicant is Turn Needle Intl., Inc.. It received FDA 510(k) clearance on 1985-04-01 under 510(k) number K850503. The device is classified under product code KMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SECU-TAPE UNIVERSAL FLEXIBLE MEDICAL CLAMPS?

SECU-TAPE UNIVERSAL FLEXIBLE MEDICAL CLAMPS is a medical device that received FDA 510(k) clearance on 1985-04-01. The listed applicant is Turn Needle Intl., Inc.. The 510(k) number is K850503.

When did SECU-TAPE UNIVERSAL FLEXIBLE MEDICAL CLAMPS receive FDA 510(k) clearance?

SECU-TAPE UNIVERSAL FLEXIBLE MEDICAL CLAMPS received FDA 510(k) clearance on 1985-04-01, under 510(k) number K850503.

Who is the listed applicant for SECU-TAPE UNIVERSAL FLEXIBLE MEDICAL CLAMPS?

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

What is the FDA product code for SECU-TAPE UNIVERSAL FLEXIBLE MEDICAL CLAMPS?

The FDA product code for SECU-TAPE UNIVERSAL FLEXIBLE MEDICAL CLAMPS is KMK.

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 Turn Needle Intl., 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.

K844917TURN NEEDLE INTRAVENOUS CANNUL, NUB, W/TUBING INTE

Related Devices (Code: KMK)

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.

K180994SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8FInterrad Medical, Inc.K981860A P HARNESSParaworks Enterprise, Ltd.K963365MULTI-PURPOSE MEDICAL TUBE HOLDERByrd Medical Devices, Inc.K941098SECURE-SITEOp-Co Medical Products , Ltd.K943147STATLOCK CVVenetec, Inc.K943047IV START KITSSterile Concepts, 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.

↑