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)

SHARPS CADDY MAGNETIC & SHARPS CADDY FOA

K-Number: K802866 · 1980-11-17

ApplicantInstranetics, Inc.
Decision Date1980-11-17
Product CodeKDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SHARPS CADDY MAGNETIC & SHARPS CADDY FOA is the device name listed in this FDA 510(k) record. The listed applicant is Instranetics, Inc.. It received FDA 510(k) clearance on 1980-11-17 under 510(k) number K802866. The device is classified under product code KDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHARPS CADDY MAGNETIC & SHARPS CADDY FOA?

SHARPS CADDY MAGNETIC & SHARPS CADDY FOA is a medical device that received FDA 510(k) clearance on 1980-11-17. The listed applicant is Instranetics, Inc.. The 510(k) number is K802866.

When did SHARPS CADDY MAGNETIC & SHARPS CADDY FOA receive FDA 510(k) clearance?

SHARPS CADDY MAGNETIC & SHARPS CADDY FOA received FDA 510(k) clearance on 1980-11-17, under 510(k) number K802866.

Who is the listed applicant for SHARPS CADDY MAGNETIC & SHARPS CADDY FOA?

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

What is the FDA product code for SHARPS CADDY MAGNETIC & SHARPS CADDY FOA?

The FDA product code for SHARPS CADDY MAGNETIC & SHARPS CADDY FOA is KDC.

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 Instranetics, 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.

K823430INSTRA-SAFEK811822TIP-VUK811824CAUTERY CADDY PADK811823SHARPS CADDY FBK810294LINE CADDYK810208BLADE SAFE

View all 10 devices →

Related Devices (Code: KDC)

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.

K943229DISPOSABLE SURGICAL SCISSORS AND FORCEPSY.M.K. International Co., Ltd.K936226SURGIMED BREAST LOCALIZATION NEEDLE WIRE SETMeadox Medicals, Div. Boston Scientific Corp.K920153THERMUFF BAGTechstylesK920263MANUAL SURGICAL INSTRUMENTSPhoenix Instruments Div.K915064DISPOSABLE CAUTERY ABRASIVE PADAmerican Medical Mfg., Inc.K914960INSTRUMENT ORGANIZERO.R. 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.

↑