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

MD-1835

K Number: K964806 · Decision Mar 4, 1997
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
12
Applicant Total
69
Review Days
95

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
MD-1835
K Number
K964806
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1670
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Fischer Imaging Corp.
Date Received
November 29, 1996
Decision Date
March 4, 1997
Product Code
IXL
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
IXL Device, Spot-Film

Similar 510(k) Clearances

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

View all

Other Clearances by Fischer Imaging Corp.

K Number Device Name
K042095 MAMMOTEST
K021113 MAMMOPATH
K981414 LC POSITIONER
K973400 MAMMOTEST ADAPTER DRIVER
K961207 EP-X BIPLANE
K961022 TANGENT VI TABLE
K950291 DIGITAL 625HF
K945619 ATHENA HFX
K944147 MICRO X-50 HF
K944149 MICRO X-80 HF
Search all 69 clearances from Fischer Imaging Corp. →