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

RTLX

K Number: K992392 · Decision Mar 31, 2000
Classifications
1
FEI Numbers
87
Registration Numbers
87
Same Product Code
205
Applicant Total
14
Review Days
256

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Basic Information

Device Name
RTLX
K Number
K992392
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.1800
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Infimed, Inc.
Date Received
July 19, 1999
Decision Date
March 31, 2000
Product Code
MUH
Advisory Committee
Dental
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
MUH System, X-Ray, Extraoral Source, Digital

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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
K992794 STINGRAY DR, MODEL 1
K992575 CARDIOVASCULAR WORKSTATION, MODEL CWS 5000/CWS 3000
K962422 INFIMED DENTAL SYSTEM
K963037 PATRIOT
Search all 14 clearances from Infimed, Inc. →