Atlas FDA

AUTOMATIC POSITIVE BEAM COLLIMATOR

FDA 510(k) clearance K791504 · decided 1979-09-07

Clearance details

K-number
K791504
Device name
AUTOMATIC POSITIVE BEAM COLLIMATOR
Applicant
Dial-X Instruments, Inc.
Decision
Substantially Equivalent
Date received
1979-08-06
Decision date
1979-09-07
Days to decision
32 days
Clearance type
Traditional
Product code
KPW
Device class
2
Regulation number
892.1610
Medical specialty
Radiology
Advisory committee
Radiology
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
LUMOS, MODEL R 72B (K093596)Lumos, Inc.2010-01-12
COLLIMATOR, MODEL M-38 (K062788)Umi International2006-12-28
R 72 (K030487)Ralco S.R.L.2003-08-01
BLA-800A (K954310)Toshiba Medical Systems1995-10-18
R 302 (K946320)Ralco S.R.L.1995-05-11
P2020-8-0 BEAM-LIMITING DEVICE (K914184)Precise Optics1991-11-27
DENSICOMP 250 (K904587)L. Keroack Co.1991-01-24
TF-63SA (K904044)Toshiba America Medical Systems, In.C1990-11-29
EUREKA EXTENSION CYLINDERS (K904489)Eureka X-Ray Tube Corp.1990-10-15
RALCO COLLIMATOR, AUTOMATIC RADIOGRAPHIC (K820306)Tecnomed, Inc.1982-03-05
RALCO COLLIMATORS, MANUAL RADIOGRAPHIC (K820305)Tecnomed, Inc.1982-03-04
PODIOSCOPE BY ARROW (K820119)Arrow X-Ray Corp.1982-02-18

Recalls involving this device

No recalls on record reference this clearance.