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

ARTHROSCOPY PUMP, MODEL A107

K Number: K030402 · Decision Apr 17, 2003
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
680
Applicant Total
15
Review Days
70

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
ARTHROSCOPY PUMP, MODEL A107
K Number
K030402
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
W.O.M. World of Medicine AG
Date Received
February 6, 2003
Decision Date
April 17, 2003
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 W.O.M. World of Medicine AG

K Number Device Name
K123732 HYSTEROSCOPY PUMP HM6
K112642 AQUILEX FLUID CONTROL SYSTEM H112
K063367 45L CORE INSUFFLATOR, MODEL F114
K062380 FLOSIMPLE ARTHROSCOPY PUMP A120
K060723 40 L HIGH FLOW INSUFFLATOR F113
K042457 URO PRO
K030837 40 L HIGH FLOW INSUFFLATOR F108
K033927 ARTHOSCOPY PUMP A115
K032023 W.O.M. LASER U100PLUS
K022721 UROPOWER
Search all 15 clearances from W.O.M. World of Medicine AG →