FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ARTHROSCOPES

K Number: K003831 · Decision Jul 20, 2001
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
680
Applicant Total
7
Review Days
221

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
ARTHROSCOPES
K Number
K003831
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Global Endoscopy, Inc.
Date Received
December 11, 2000
Decision Date
July 20, 2001
Product Code
HRX
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HRX Arthroscope

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HRX), ordered by most recent decision date.

View all

Other Clearances by Global Endoscopy, Inc.

K Number Device Name
K003805 GYNECOLOGICAL LAPAROSCOPES
K003802 HYSTEROSCOPES
K003830 ENT ENDOSCOPES
K003803 GENERAL SURGICAL LAPAROSCOPES
K003806 URETEROSCOPES
K003807 CYSTOSCOPES