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)

RESECTOSCOPE ELECTRO CAUTERY CUTTING LOOP

K-Number: K943879 · 1995-02-07

Decision Date1995-02-07
Product CodeFAS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

RESECTOSCOPE ELECTRO CAUTERY CUTTING LOOP is the device name listed in this FDA 510(k) record. The listed applicant is American Urologicals, Inc.. It received FDA 510(k) clearance on 1995-02-07 under 510(k) number K943879. The device is classified under product code FAS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESECTOSCOPE ELECTRO CAUTERY CUTTING LOOP?

RESECTOSCOPE ELECTRO CAUTERY CUTTING LOOP is a medical device that received FDA 510(k) clearance on 1995-02-07. The listed applicant is American Urologicals, Inc.. The 510(k) number is K943879.

When did RESECTOSCOPE ELECTRO CAUTERY CUTTING LOOP receive FDA 510(k) clearance?

RESECTOSCOPE ELECTRO CAUTERY CUTTING LOOP received FDA 510(k) clearance on 1995-02-07, under 510(k) number K943879.

Who is the listed applicant for RESECTOSCOPE ELECTRO CAUTERY CUTTING LOOP?

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

What is the FDA product code for RESECTOSCOPE ELECTRO CAUTERY CUTTING LOOP?

The FDA product code for RESECTOSCOPE ELECTRO CAUTERY CUTTING LOOP is FAS.

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.

Related Devices (Code: FAS)

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.

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.

↑