Atlas FDA

ELECTRODE/EXTENSION CABLES, MODELS ATAR

FDA 510(k) clearance K070926 · decided 2007-06-07

Clearance details

K-number
K070926
Device name
ELECTRODE/EXTENSION CABLES, MODELS ATAR
Applicant
Oscor, Inc.
Decision
Substantially Equivalent
Date received
2007-04-03
Decision date
2007-06-07
Days to decision
65 days
Clearance type
Special
Product code
IKD
Device class
2
Regulation number
890.1175
Medical specialty
Physical Medicine
Advisory committee
Physical Medicine
Location
Palm Harbor, FL, 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
THE LEADAWAY (K992372)Therapy Equipment, Inc.1999-10-13
PHYSIOMETRIX CABLE ADAPTER MODIFICATION (K935260)Physiometrix, Inc.1993-12-23
LIFE-SPAN CABLE (K873361)Chemfet Corp.1987-11-09
CLEAR LEADS-RADIOTRANSPARENT WIRES (K834583)Quinton, Inc.1984-01-30
R2 ESU CABLE-ADAPTER MODELS 160,161 (K800934)R2 Corp.1980-05-20

Recalls involving this device

RecordFirmDate
ATAR Reusable Extension Cable, sold under brand names: ATAR Reusable Series, ATAR 53912 Re recall (Z-2340-2017)Oscor, Inc.2017-04-10
ATAR Disposable Extension Cable, sold under brand names: ATAR Disposable Series, ATAR 5391 recall (Z-2733-2017)Oscor, Inc.2017-04-10