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

MODIFICATION TO HYDROCISION DEBRIDEMENT SYSTEM

K Number: K011612 · Decision Jun 22, 2001
Classifications
1
FEI Numbers
146
Registration Numbers
146
Same Product Code
52
Applicant Total
12
Review Days
28

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Basic Information

Device Name
MODIFICATION TO HYDROCISION DEBRIDEMENT SYSTEM
K Number
K011612
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
880.5475
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hydrocision, Inc.
Date Received
May 25, 2001
Decision Date
June 22, 2001
Product Code
FQH
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FQH Lavage, Jet

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Other Clearances by Hydrocision, Inc.

K Number Device Name
K241990 SpineSite Endoscope System
K200729 HydroCision SpineJet System
K190804 HydroCision TenJet Device
K041233 ARTHROJET XT
K032529 HYDROCISION ARTHROJET SYSTEM WITH CAUTERY, TURBOBURR AND CURETTE, MODELS 51300, 51310
K021813 HYDROCISION GENERAL SURGERY FLUIDJET SYSTEM
K020688 HYDROCISION ARTHOJET SYSTEM WITH CAUTERY AND TURBOBURR
K002764 HYDROCISION ARTHROJET SYSTEM WITH CAUTERY AND BURR
K991383 HYDROCISION DEBDRIDEMENT SYSTEM
K993009 HYDROCISION ARTHROJET SYSTEM WITH CAUTERY
Search all 12 clearances from Hydrocision, Inc. →