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510(k) K840036

FITEX by Britt Corp., Inc.

K840036 is an FDA 510(k) premarket notification submitted by Britt Corp., Inc. for the device "FITEX". The FDA issued a decision of Substantially Equivalent on October 26, 1984. Britt Corp., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 26, 1984
Date Received
January 5, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Britt Corp., Inc.

  • K003828 — VASO PRESS DVT FOOT GARMENT #VP 520 (May 18, 2001)
  • K991038 — VASO PRESS DVT SYSTEM, MODELS VP500, VP501 (June 22, 2000)
  • K974393 — VASO PRESS SYSTEM (March 19, 1999)
  • K860977 — MODEL 545-45 FOR NEUROLOGICAL SURGICAL APPLICATION (October 16, 1986)
  • K860975 — MODEL 545-45 LASER FOR EAR, NOSE & THROAT (July 18, 1986)
  • K860974 — MODEL 545-45 LASER FOR DERMA., POD., SURGICAL (July 7, 1986)
  • K860277 — MODEL 525-25 WATT C02 LASER FOR EAR, NOSE & THROAT (May 6, 1986)
  • K860273 — MODEL 525 - 25 WATT CO2 MEDICAL LASER/PODIATRY (April 23, 1986)
  • K860278 — MODEL 525-25 WATT CO2 LASER FOR DERMA/PLASTIC (April 15, 1986)
  • K851425 — MODEL J25-25 WATT CO2 LASER (November 12, 1985)

FDA data resources