Atlas FDA

COLLIMATOR MODEL A280BLMD & MODEL A280BLMP

FDA 510(k) clearance K861941 · decided 1986-07-25

Clearance details

K-number
K861941
Device name
COLLIMATOR MODEL A280BLMD & MODEL A280BLMP
Applicant
D&R X-Ray Products, Inc.
Decision
Substantially Equivalent
Date received
1986-05-20
Decision date
1986-07-25
Days to decision
66 days
Clearance type
Traditional
Product code
IZX
Device class
2
Regulation number
892.1610
Medical specialty
Radiology
Advisory committee
Radiology
Location
Richmond, VA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

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RecordFirmDate
RALCO (K110856)Ralco S.R.L.2011-08-10
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SHIMADZU COLLIMATOR R-20J (K042840)Shimadzu Corp.2004-12-03
SHIMADZU COLLIMATOR R-30H (K031771)Shimadzu Corp.2003-08-21
FACTS MONOBLOCK (K981267)Dynarad Corp.1998-05-06
LIGHTLINE-M (K974240)Wuestec Medical, Inc.1997-12-22
AXT 150M MANUAL COLLIMATOR (AXT 150M) (K972966)Applied X-Ray Technologies, Inc.1997-08-21
RINN UNIVERSAL COLLIMATOR (K932134)Rinn Corp.1993-07-26
MODEL MGB-301 DIAPHRAGM FILM 24 X 30 CM (K912180)Instrumentarium Imaging, Inc.1991-10-21
R-100-ET MANUAL COLLIMATOR (K900007)Advantech1990-02-06
R-150-ET COLLIMATOR (K896486)Advantech1990-01-23
COLLI-MATETM MODEL NO. B800 (K874687)Summit Industries, Inc.1987-12-30

Recalls involving this device

No recalls on record reference this clearance.