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)

AESCULAP'S MODULAR ENDOSCOPIC INSTRUMENTS FOR GYNECOLOGY

K-Number: K010752 · 2001-06-11

ApplicantAesculap, Inc.
Decision Date2001-06-11
Product CodeKNF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

AESCULAP'S MODULAR ENDOSCOPIC INSTRUMENTS FOR GYNECOLOGY is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2001-06-11 under 510(k) number K010752. The device is classified under product code KNF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AESCULAP'S MODULAR ENDOSCOPIC INSTRUMENTS FOR GYNECOLOGY?

AESCULAP'S MODULAR ENDOSCOPIC INSTRUMENTS FOR GYNECOLOGY is a medical device that received FDA 510(k) clearance on 2001-06-11. The listed applicant is Aesculap, Inc.. The 510(k) number is K010752.

When did AESCULAP'S MODULAR ENDOSCOPIC INSTRUMENTS FOR GYNECOLOGY receive FDA 510(k) clearance?

AESCULAP'S MODULAR ENDOSCOPIC INSTRUMENTS FOR GYNECOLOGY received FDA 510(k) clearance on 2001-06-11, under 510(k) number K010752.

Who is the listed applicant for AESCULAP'S MODULAR ENDOSCOPIC INSTRUMENTS FOR GYNECOLOGY?

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

What is the FDA product code for AESCULAP'S MODULAR ENDOSCOPIC INSTRUMENTS FOR GYNECOLOGY?

The FDA product code for AESCULAP'S MODULAR ENDOSCOPIC INSTRUMENTS FOR GYNECOLOGY is KNF.

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 Aesculap, 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.

K242762Aesculap Aicon® Series Container SystemK242003XABO Ventricular Catheter, XABO Peritoneal Catheter, XABO Catheter SetK223596SQ.line KERRISONK214041Aesculap AICON ContainerK211572Aesculap Slim Clip ApplierK203739ELAN 4 Electro Motor System

View all 195 devices →

Related Devices (Code: KNF)

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.

K254303KARL STORZ SUPRALOOPKarl Storz SE & CO. KGK250705Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.K240503Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.K233848Sonata Transcervical Fibroid Ablation System 2.2 (SONATA2-220)Gynesonics, Inc.K222304Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.K211535Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, 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.

↑