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510(k) K837046

AUTOFOCUS PROBE FOR USE WITH ULTRASOUND AUTOSECTOR SYSTEM by Technicare Corp.

K837046 is an FDA 510(k) premarket notification submitted by Technicare Corp. for the device "AUTOFOCUS PROBE FOR USE WITH ULTRASOUND AUTOSECTOR SYSTEM". The FDA issued a decision of Substantially Equivalent on April 1, 1983. Technicare Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 1, 1983
Date Received
January 10, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Technicare Corp.

  • K854340 — TECHNICARE 720 HPS CT SCANNER (November 15, 1985)
  • K852089 — SATURN NUCLEAR MEDICINE COMPUTER SYSTEM (July 18, 1985)
  • K844293 — AUTO DII MULTI FREQUENCY (February 13, 1985)
  • K844247 — ULTRASONIC SCANNER CALIBRATION & TEST PHANTOMS (January 23, 1985)
  • K843716 — NUCLEAR 700 MEDICINE MECHANICAL POSIT- (December 17, 1984)
  • K842777 — AUTOFOCUS DUAL ELEMENT PROBE (November 29, 1984)
  • K841817 — TECHNICARE 248 SL & 260SL (August 17, 1984)
  • K840860 — CENTAURI CT SCANNER (May 22, 1984)
  • K840540 — TECHNICARE MODEL 330 (May 9, 1984)
  • K834486 — TECHNICARE 280 (April 13, 1984)

FDA data resources