Atlas FDA

GENERAL EQUIPMENT COVER

FDA 510(k) clearance K782155 · decided 1979-01-17

Clearance details

K-number
K782155
Device name
GENERAL EQUIPMENT COVER
Applicant
Contour Fabricators, Inc.
Decision
Substantially Equivalent
Date received
1978-12-22
Decision date
1979-01-17
Days to decision
26 days
Clearance type
Traditional
Product code
IZL
Device class
2
Regulation number
892.1720
Medical specialty
Radiology
Advisory committee
Radiology
Location
Fenton, MI, US
Third-party review
No
Expedited review
No

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Recalls involving this device

RecordFirmDate
GE Medical Systems, OEC, Vascular Drape, 00-902776-01, Sterile. 150" long x 87" wide. Dist recall (Z-1706-2009)GE Medical Systems, LLC2009-09-01
Sterile, Drape, Headset, Lower, Part Number 888944-01. recall (Z-1707-2009)GE Medical Systems, LLC2009-09-01
Sterile, Drape, Headset, Upper, Part Number 888945-01. recall (Z-1708-2009)GE Medical Systems, LLC2009-09-01
Disposable Pack, Headset Part Number 888946-01(kit includes Part Number 888944-01, Sterile recall (Z-1709-2009)GE Medical Systems, LLC2009-09-01
GE Healthcare, Drapes and Sterile Covers PART NUMBER DESCRIPTION 00-900352-01 DRAIN BAG W/ recall (Z-1730-2009)GE Medical Systems, LLC2009-08-14