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510(k) K834577

I/A PROBE LINES by Frigitronics of Connecticut, Inc.

K834577 is an FDA 510(k) premarket notification submitted by Frigitronics of Connecticut, Inc. for the device "I/A PROBE LINES". The FDA issued a decision of Substantially Equivalent on May 22, 1984. Frigitronics of Connecticut, Inc. has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 22, 1984
Date Received
December 29, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Frigitronics of Connecticut, Inc.

  • K891282 — MIC-100 WITH CRYOPROBES (June 15, 1989)
  • K872362 — FRIGITRONICS ACC-1000 CAPSULE CUTTER (July 27, 1987)
  • K853308 — KEATES IRRIGATION/ASPIRATION/VITREOUS CUTTER 5000 (October 4, 1985)
  • K840536 — CRYO SURG 5900 (April 23, 1984)
  • K834437 — KEATES IRRIGATION/ASPIRATION/VITREOUS (March 30, 1984)
  • K822599 — KEATES I/A SYSTEM FRIGITRONICS 4000 (October 6, 1982)
  • K811390 — CCS100 CRYOSURGICAL SYSTEM (June 16, 1981)
  • K760742 — CS-76 AND/OR CRYOCARE I (November 3, 1976)

FDA data resources