FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

HYDRAJUST III UROLOGICAL TABLE

K Number: K860040 · Decision Feb 10, 1986
Classifications
1
FEI Numbers
5
Registration Numbers
5
Same Product Code
7
Applicant Total
27
Review Days
35

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
HYDRAJUST III UROLOGICAL TABLE
K Number
K860040
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.4890
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Mallinckrodt Group, Inc.
Date Received
January 6, 1986
Decision Date
February 10, 1986
Product Code
KQS
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
KQS Table, Cystometric, Non-Electric And Accessories

Similar 510(k) Clearances

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

View all

Other Clearances by Mallinckrodt Group, Inc.

K Number Device Name
K945053 LF CT HIG PRESSURE CATHETERS
K945140 URO-FLO
K943581 HYDRADJUST IV UROLOGICAL TABLE
K943122 SURGICAL DRAPES
K934664 HYDRAGOWN
K920742 HYDRAJUST IV UROLOGICAL TABLE
K912944 CT 8000 DIGITAL INJECTION SYSTEM
K913264 HYDRAVIEW 1000 DIGITAL IMAGE PROCESS/STOR DEVICE
K905789 FRANKLIN 9000 WALL STAND
K904147 HUGH YOUNG II UROLOGICAL X-RAY SYSTEM
Search all 27 clearances from Mallinckrodt Group, Inc. →