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)

NO-SCALPEL VASCETOMY INSTRUMENTS

K-Number: K922971 · 1992-09-23

ApplicantPilling Co.
Decision Date1992-09-23
Product CodeKOA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NO-SCALPEL VASCETOMY INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Co.. It received FDA 510(k) clearance on 1992-09-23 under 510(k) number K922971. 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 NO-SCALPEL VASCETOMY INSTRUMENTS?

NO-SCALPEL VASCETOMY INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1992-09-23. The listed applicant is Pilling Co.. The 510(k) number is K922971.

When did NO-SCALPEL VASCETOMY INSTRUMENTS receive FDA 510(k) clearance?

NO-SCALPEL VASCETOMY INSTRUMENTS received FDA 510(k) clearance on 1992-09-23, under 510(k) number K922971.

Who is the listed applicant for NO-SCALPEL VASCETOMY INSTRUMENTS?

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

What is the FDA product code for NO-SCALPEL VASCETOMY INSTRUMENTS?

The FDA product code for NO-SCALPEL VASCETOMY INSTRUMENTS 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 Pilling Co. 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.

K934427PILLING LAPAROSCOPIC INSTRUMENTATIONK925370TRIANGULAR JAW MICROLARYNGEAL FORCEPSK925198KAISER NO CANNULA THORACOSCOPY/LAPAROSCOPY INSTRK914015CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMPK911099MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINEK911100MEHIGAN-PILLING PHLEBETOME TM

View all 39 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.

↑