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

EBICE

K Number: K953532 · Decision Oct 4, 1995
Classifications
1
FEI Numbers
123
Registration Numbers
123
Same Product Code
92
Applicant Total
28
Review Days
69

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
EBICE
K Number
K953532
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5720
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Electro-Biology, Inc.
Date Received
July 27, 1995
Decision Date
October 4, 1995
Product Code
ILO
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
ILO Pack, Hot Or Cold, Water Circulating

Similar 510(k) Clearances

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

View all

Other Clearances by Electro-Biology, Inc.

K Number Device Name
K992333 EBI OMEGA 21 SYSTEM
K992367 EBI XFIX DYNAFIX SYSTEM HA COATED SCREWS
K991941 EBI XFIX DFS RAIL SYSTEM
K991092 EBI SPINELINK ANTERIOR CERVICAL SPINAL SYSTEM
K990303 EBI OMEGA 21 SYSTEM
K990459 EBI VUECATH ENDOSCOPIC SYSTEN
K990999 MODIFICATION OF: EBI SPINELINK SYSTEM
K984027 EBI SPINELINK SYSTEM
K982484 EBI VUECATH ENDOSCOPIC SPINAL SYSTEM
K982908 MODIFICATION TO EBI SPINELINK SYSTEM
Search all 28 clearances from Electro-Biology, Inc. →