Brentwood Instruments, Inc.
Brentwood Instruments, Inc. holds FDA 510(k) medical device clearances, first cleared 1981, most recent 1990.
Top product codes for Brentwood Instruments, Inc.
Recent clearances by Brentwood Instruments, Inc.
- K896924 — SPIROSCAN 4000
- K882366 — RHYTHMSCAN HR HOLTER RECORDER
- K871572 — RHYTHMSCAN
- K860024 — FUKUDA DENSHI CARDIMAX FCP-211
- K853979 — CARDIMAX FX-1164
- K854505 — CARDIMAX FX-406U
- K851135 — SPIRO SCAN
- K851123 — R-1000 ECG RECEIVER
- K851124 — T-1000 ECG TRANSMITTER
- K842976 — BRENTWOOD EZ SCAN 200 AMBULATORY ECG
- K844470 — FUKUDA DENSHI MODEL FCP-220
- K833594 — FUKUDA DENSHI FX-302 AUTO/THREE CHAN
- K833593 — FUKUDA DENSHI FX-102 AUTO-SINGLE CHAN
- K842169 — FCP-11ECG
- K830907 — AMBULATORY ECG EVENT RECORDER
- K823585 — COMPUTER-AIDED ELECTROCARDIOGRAPH FCP-13
- K823586 — COMPUTER-AIDED ELECTROCARDIOGRAPH FCP200
- K823584 — FUKUDA DENSHI 6-CHANNEL AUTO. ELECTRO-
- K813021 — FUKUDA DENSHI...ELECTROCARDIOGRAPH FD-36
- K813022 — FUKUDA DENSHI CARDIMAX FK-12
- K813023 — FUKUDA DENSHI CARDIMAX FK-11
Data sourced from openFDA. This site is unofficial and independent of the FDA.