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510(k) K827993

MTH C/A MOBILE C ARM by General Medical Merate S.P.A

K827993 is an FDA 510(k) premarket notification submitted by General Medical Merate S.P.A for the device "MTH C/A MOBILE C ARM". The FDA issued a decision of Substantially Equivalent on September 13, 1982. General Medical Merate S.P.A has at least 6 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 13, 1982
Date Received
August 24, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by General Medical Merate S.P.A

  • K213081 — CLISIS SYSTEMS, Discovery RF180 (October 26, 2021)
  • K173395 — MECALL CLISIS SYSTEMS, Discovery RF180 (May 21, 2018)
  • K140380 — OPERA SWING (September 26, 2014)
  • K082243 — PRECISION RXI ANALOG AND DIGITAL X-RAY SYSTEMS (November 7, 2008)
  • K041605 — PRECISION RXI ANALOG X-RAY SYSTEM (June 30, 2004)
  • K881386 — X-RAY GENERATING SYSTEM TF 1000 (July 8, 1988)

FDA data resources