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)

ELEVATORS-COTTLE,MCKENTY,GOLDMAN,JOSEPH,CONVERSE

K-Number: K891894 · 1989-04-12

ApplicantZinnanti Surgical Instruments, Inc.
Decision Date1989-04-12
Product CodeGEG
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELEVATORS-COTTLE,MCKENTY,GOLDMAN,JOSEPH,CONVERSE is the device name listed in this FDA 510(k) record. The listed applicant is Zinnanti Surgical Instruments, Inc.. It received FDA 510(k) clearance on 1989-04-12 under 510(k) number K891894. The device is classified under product code GEG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELEVATORS-COTTLE,MCKENTY,GOLDMAN,JOSEPH,CONVERSE?

ELEVATORS-COTTLE,MCKENTY,GOLDMAN,JOSEPH,CONVERSE is a medical device that received FDA 510(k) clearance on 1989-04-12. The listed applicant is Zinnanti Surgical Instruments, Inc.. The 510(k) number is K891894.

When did ELEVATORS-COTTLE,MCKENTY,GOLDMAN,JOSEPH,CONVERSE receive FDA 510(k) clearance?

ELEVATORS-COTTLE,MCKENTY,GOLDMAN,JOSEPH,CONVERSE received FDA 510(k) clearance on 1989-04-12, under 510(k) number K891894.

Who is the listed applicant for ELEVATORS-COTTLE,MCKENTY,GOLDMAN,JOSEPH,CONVERSE?

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

What is the FDA product code for ELEVATORS-COTTLE,MCKENTY,GOLDMAN,JOSEPH,CONVERSE?

The FDA product code for ELEVATORS-COTTLE,MCKENTY,GOLDMAN,JOSEPH,CONVERSE is GEG.

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 Zinnanti Surgical Instruments, 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.

K925501NYLON COATED SPECULAK941458UTERINE MANIPULATOR/INJECTOR WITH SPRINGK941457UTERINE INJECTOR WITH SPRINGK925560ZSI LOOP, ZSI BALL & ZSI NEEDLE ELECTRODESK925957SCISSORS FOR LAPAROSCOPIC SURGERY OB/GYN USEK925960FORCEPS FOR LAPAROSCOPIC SURGERY OB/GYN USE

View all 76 devices →

Related Devices (Code: GEG)

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.

K891899ELEVATORS, VARIOUS TYPESZinnanti Surgical Instruments, Inc.K890365SEPTUM ELEVATORKinetic Medical ProductsK890253SURGICAL ELEVATORKinetic Medical ProductsK890230LIGATURE NEEDLESKinetic Medical ProductsK8724911.1 TWIST DRILLS AND 1.2 CORTICAL DRILLSMicro-Aire Surgical Instruments, Inc.K870781ACROMED WALLIE-HEINIG DISECTOR/ELEVATORSBuckman Co., 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.

↑