Britt Corp., Inc.
Britt Corp., Inc. holds FDA 510(k) medical device clearances, first cleared 1979, most recent 2001.
Top product codes for Britt Corp., Inc.
Recent clearances by Britt Corp., Inc.
- K003828 — VASO PRESS DVT FOOT GARMENT #VP 520
- K991038 — VASO PRESS DVT SYSTEM, MODELS VP500, VP501
- K974393 — VASO PRESS SYSTEM
- K860977 — MODEL 545-45 FOR NEUROLOGICAL SURGICAL APPLICATION
- K860975 — MODEL 545-45 LASER FOR EAR, NOSE & THROAT
- K860974 — MODEL 545-45 LASER FOR DERMA., POD., SURGICAL
- K860277 — MODEL 525-25 WATT C02 LASER FOR EAR, NOSE & THROAT
- K860273 — MODEL 525 - 25 WATT CO2 MEDICAL LASER/PODIATRY
- K860278 — MODEL 525-25 WATT CO2 LASER FOR DERMA/PLASTIC
- K851425 — MODEL J25-25 WATT CO2 LASER
- K840020 — FITNESS LOGGER
- K840036 — FITEX
- K833533 — LASER PHOTOCOAGULATOR 1520-A & K
- K837200 — BRITT SURGICAL PHOTOCOAGULATOR SYSTEM
- K837151 — BLUE GREEN FILTER SYSTEM TO MODEL 152 AND 150 LASER SYSTEM
- K813492 — BRITT KRYPTON LASERS 150K & 152K
- K790694 — BRITT LENS COMPUTER
Data sourced from openFDA. This site is unofficial and independent of the FDA.