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

SC1000 SCAN CONVERTER

K Number: K926348 · Decision Nov 19, 1993
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
54
Applicant Total
14
Review Days
337

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
SC1000 SCAN CONVERTER
K Number
K926348
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.2010
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Perkins Mfg. Co.
Date Received
December 17, 1992
Decision Date
November 19, 1993
Product Code
LMB
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
LMB Device, Digital Image Storage, Radiological

Similar 510(k) Clearances

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

View all

Other Clearances by Perkins Mfg. Co.

K Number Device Name
K972136 TV MONITOR (P12/17)
K954222 VIDEO ENHANCEMENT UNIT
K920550 DISPLAY PROCESSOR - MODEL IDP5100
K915232 GRUNDIG ELECTRONICS VARIOUS MODELS
K910384 VIDEO ANNOTATOR MODEL PK2310
K904986 PROGRAMMABLE VIDEO CONTROLLER MODEL PK2060
K904540 VIDEO SYSTEM INTERFACE MODELS
K896615 CINE CAMERA CONTROL MODEL PK2037
K895500 PATIENT POSITIONING ACCESSORIES
K893644 PK2025/PK2045 PROGRAMMABLE VIDEO CONTROLLER
Search all 14 clearances from Perkins Mfg. Co. →