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

JACKSON HYDRO SYSTEM

K Number: K802780 · Decision Dec 10, 1980
Classifications
1
FEI Numbers
58
Registration Numbers
58
Same Product Code
20
Applicant Total
16
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
JACKSON HYDRO SYSTEM
K Number
K802780
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5500
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
S. Jackson, Inc.
Date Received
November 5, 1980
Decision Date
December 10, 1980
Product Code
FNG
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
FNG Lift, Patient, Ac-Powered

Similar 510(k) Clearances

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

View all

Other Clearances by S. Jackson, Inc.

K Number Device Name
K080216 SUPRAMESH EXTRA
K973379 STERILE SUPRAFOIL SMOOTH NYLON FOIL SHEETS
K931614 MOPYLEN SUTURE
K931613 SUPRAMID SUTURE
K931612 NYLAMID SUTURE
K922630 MOPYLEN
K912429 N80-838 SUPRAMID EXTRA SUTURE
K904052 SUPRAMID EXTRA SUTURES
K852011 NYLAMID MESH PAD FULL & HALF
K831725 FOIL IN 3 FORMS-NON-STERILE SHEETS
Search all 16 clearances from S. Jackson, Inc. →