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510(k) K013290

MODIFIED 650 MAMMOGRAPHY SYSTEM by Lorad, A Hologic Co. — Product Code IZH

K013290 is an FDA 510(k) premarket notification submitted by Lorad, A Hologic Co. for the device "MODIFIED 650 MAMMOGRAPHY SYSTEM". The FDA issued a decision of Substantially Equivalent on October 24, 2001. The device falls under product code IZH (System, X-Ray, Mammographic), a Class II device regulated under 21 CFR 892.1710. Lorad, A Hologic Co. has at least 4 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 24, 2001
Date Received
October 2, 2001
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, X-Ray, Mammographic
Device Class
Class II
Regulation Number
892.1710
Review Panel
RA
Submission Type

Other clearances by Lorad, A Hologic Co.

  • K122836 — AFFIRM BREAST BIOPSY GUIDANCE SYSTEM (January 11, 2013)
  • K071542 — DIGITAL STEREOLOC II (July 5, 2007)
  • K030666 — MULTICARE PLATINUM SYSTEM AND ACCESSORIES (March 25, 2003)
  • K011987 — MODIFIED M-IV MAMMOGRAPHY SYSTEM (July 11, 2001)

Other clearances for product code IZH

  • K203509 — SMART FINDER (July 14, 2021)
  • K202294 — Affirm Contrast Biopsy (October 5, 2020)
  • K191495 — Biopsy Positioner (July 3, 2019)
  • K161575 — Affirm Lateral Arm Upright Biopsy Accessory (August 10, 2016)
  • K161920 — Comfort Cover (July 15, 2016)
  • K153486 — Affirm Prone Biopsy System (April 1, 2016)
  • K152038 — MammoGRIP (December 22, 2015)
  • K122836 — AFFIRM BREAST BIOPSY GUIDANCE SYSTEM (January 11, 2013)
  • K123414 — SPECBOARD JR. (January 11, 2013)
  • K113607 — BIOPSY DIGIT S BIOPSY SL (August 10, 2012)

FDA data resources