Medical Device Manufacturer · US , Bellaire , TX

Prucka Engineering, Inc.

6 submissions · 6 cleared · Since 1989
6
Total
6
Cleared
0
Denied

Prucka Engineering, Inc. has 6 FDA 510(k) cleared medical devices. Based in Bellaire, US.

Historical record: 6 cleared submissions from 1989 to 2000. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Prucka Engineering, Inc. Filter by specialty or product code using the sidebar.

6 devices
1–6 of 6
PRUCKA ENGINEERING INC. CARDIOLAB EP SYSTEM,VERSION 4.2
K993414 · DPS Electrocardiograph · Cardiovascular
Apr 2000 178d
CARDIOCATH CATHETERIZATION LAB SYSTEM
K960321 · DPS Electrocardiograph · Cardiovascular
Aug 1996 212d
PEI PLAQUE ELECTRODE ARRAY
K904747 · DRF Catheter, Electrode Recording, Or Probe, Electrode Recording · Cardiovascular
Oct 1991 355d
CARDIOLAB AMPLIFIER MODULE (CAM)
K910307 · DRR Amplifier And Signal Conditioner, Biopotential · Cardiovascular
Apr 1991 78d
PE ELECTROPHYSIOLOGY LAB SYSTEM (PEEP)
K902716 · DQK Computer, Diagnostic, Programmable · Cardiovascular
Sep 1990 76d
PE INTERCARDIAC MAPPING SYSTEM (ICMS)
K895916 · DRF Catheter, Electrode Recording, Or Probe, Electrode Recording · Cardiovascular
Dec 1989 64d
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