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)

MARTIN MEDICAL PRO-SCOPE ANOSCOPE

K-Number: K863273 · 1986-11-04

ApplicantMartin Medical
Decision Date1986-11-04
Product CodeKOA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MARTIN MEDICAL PRO-SCOPE ANOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Martin Medical. It received FDA 510(k) clearance on 1986-11-04 under 510(k) number K863273. The device is classified under product code KOA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARTIN MEDICAL PRO-SCOPE ANOSCOPE?

MARTIN MEDICAL PRO-SCOPE ANOSCOPE is a medical device that received FDA 510(k) clearance on 1986-11-04. The listed applicant is Martin Medical. The 510(k) number is K863273.

When did MARTIN MEDICAL PRO-SCOPE ANOSCOPE receive FDA 510(k) clearance?

MARTIN MEDICAL PRO-SCOPE ANOSCOPE received FDA 510(k) clearance on 1986-11-04, under 510(k) number K863273.

Who is the listed applicant for MARTIN MEDICAL PRO-SCOPE ANOSCOPE?

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

What is the FDA product code for MARTIN MEDICAL PRO-SCOPE ANOSCOPE?

The FDA product code for MARTIN MEDICAL PRO-SCOPE ANOSCOPE is KOA.

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 Martin Medical 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.

K873723PLASTER VACUUM, 230V MODEL NO. 4183-161K873721PLASTER VACUUM, 115V MODEL NO. 4183-160K873719CAST CUTTER, 115V MODEL NO. 4183-106K873716ADULT WALKING HEEL PRODUCT NO. 4183-130K873722PEDESTAL WALKING HEEL PRODUCT NO. 4183-133K873720CAST CUTTER, 230V MODEL NO. 4183-107

View all 14 devices →

Related Devices (Code: KOA)

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.

K182664FiXcisionAgency For Medical Innovations GmbHK950267URETHRAL SUTURE GUIDEApplied Medical ResourcesK932465LI VASECTOMYFemcare , Ltd.K921546VASOVASOSTOMY SETCook Urological, Inc.K931181VESITEC SUTURE PASSERVesitec Medical, Inc.K921304DDV LIGATORNorth American Medical, 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.

↑