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

INFINET

K Number: K961689 · Decision Jul 31, 1996
Classifications
1
FEI Numbers
148
Registration Numbers
148
Same Product Code
141
Applicant Total
14
Review Days
91

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
INFINET
K Number
K961689
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.2020
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Infimed, Inc.
Date Received
May 1, 1996
Decision Date
July 31, 1996
Product Code
LMD
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
LMD System, Digital Image Communications, Radiological

Similar 510(k) Clearances

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

View all

Other Clearances by Infimed, Inc.

K Number Device Name
K112180 I5 DIGITAL X-RAY IMAGING SYSTEM (WITH SDX-4336CP)
K111344 I5 DIGITAL X-RAY IMAGING SYSTEM (WITH FLAATZ 560)
K103416 NEXUS DRF DIGITAL X-RAY IMAGING SYSTEM
K101833 INFISTITCH FOR I5 DIGITAL X-RAY IMAGING SYSTEM, MODEL I5
K093066 I5 DIGITAL X-RAY IMAGING SYSTEM, MODEL I5
K012490 ORION DIGITAL IMAGING SYSTEM
K992392 RTLX
K992794 STINGRAY DR, MODEL 1
K992575 CARDIOVASCULAR WORKSTATION, MODEL CWS 5000/CWS 3000
K962422 INFIMED DENTAL SYSTEM
Search all 14 clearances from Infimed, Inc. →