FDA Data MCP
☰
Docs
Datasets
Pricing
Blog
Account
Statistics
Get API Key
Home
/
510(k) Clearances
/ K840036
510(k) K840036
FITEX by
Britt Corp., Inc.
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)