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510(k) K827126

TECHNOMED GENERATOR, RADIOGRAPHIC, 3 PHASE by Tecnomed, Inc.

K827126 is an FDA 510(k) premarket notification submitted by Tecnomed, Inc. for the device "TECHNOMED GENERATOR, RADIOGRAPHIC, 3 PHASE". The FDA issued a decision of Substantially Equivalent on March 5, 1982. Tecnomed, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 5, 1982
Date Received
February 4, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Tecnomed, Inc.

  • K892226 — TEC 6340 90/15 RADIOGRAPHIC/FLUOROSCOPIC TABLE (April 26, 1989)
  • K854203 — TEC 2720 MAMEX DC MAG (March 6, 1986)
  • K820307 — TECNOMED GENERATOR, RADIOGRAPH., 3 PHASE (March 5, 1982)
  • K820306 — RALCO COLLIMATOR, AUTOMATIC RADIOGRAPHIC (March 5, 1982)
  • K827124 — RALCO COLLIMATOR, AUTOMATIC, RADIOGRAPHIC (March 5, 1982)
  • K827125 — RALCO COLLIMATORS, MANUAL, RADIOGRAPHIC (March 4, 1982)
  • K820305 — RALCO COLLIMATORS, MANUAL RADIOGRAPHIC (March 4, 1982)
  • K811197 — SUPERIX 120 (June 9, 1981)
  • K811195 — ARGOSTAT (June 9, 1981)
  • K811196 — ALLMEC 90/15 (June 9, 1981)

FDA data resources