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

ISOSTATION ANKLE/SUBTALAR MACHINE A-100

K Number: K844060 · Decision Nov 23, 1984
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
60
Applicant Total
6
Review Days
36

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
ISOSTATION ANKLE/SUBTALAR MACHINE A-100
K Number
K844060
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.1925
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Isotechnologies, Inc.
Date Received
October 18, 1984
Decision Date
November 23, 1984
Product Code
IKK
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
IKK System, Isokinetic Testing And Evaluation

Similar 510(k) Clearances

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

View all

Other Clearances by Isotechnologies, Inc.

K Number Device Name
K933063 ISOTECHNOLOGIES BACK TRACKER AND BACK WORKS SOFTWA
K912175 ISOTECHNOLOGIES LIFTSTATION & LIFTWORKS SOFTWARE
K854621 ISOSTATION KNEE MACHINE (K-100)
K842296 ISOSTATION LOWER BACK MACHINE
K841849 ISOSTATION SHOULDER MACHINE