Andries Physical Assessment Computer

FDA 510(k) K870545 · Andries Tek, Inc.

Substantially Equivalent

510(k) numberK870545

Submission

Device name
Andries Physical Assessment Computer
Applicant
Andries Tek, Inc.
Austin, TX, US
Received
February 10, 1987
Decision date
August 14, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DQC – Phonocardiograph
Device class
Class I (low risk)
Regulation
21 CFR 870.2390
Specialty
Cardiovascular

Other 510(k)s with product code DQC

510(k)DeviceApplicantDecision
K950537Cardiophonics Incorporated DPS 2000 PhonocardiographDQC · Traditional Cardiophonics, Inc.03/01/1996SE
K952651Life Sound SensorDQC · Traditional Flowscan, Inc.09/19/1995SE
K943726Acoustic RecorderDQC · Traditional Technology Applications Assoc., Inc.11/30/1994SE
K924054PhonocardiographDQC · Traditional Echo Ultrasound01/22/1993SE
K902185Dynamic Spectral PhonocardiographDQC · Traditional Reeves Scientific, Inc.03/25/1991SE
K900560Acuson Heartsound/Pulse/Respiration ModuleDQC · Traditional Acuson Corp.12/03/1990SE
K900365Pag Microprocessor-Controlled ModuleDQC · Traditional Life Sciences Manufacturing, Inc.07/18/1990SE
K873640Modified DSP100 AmplifierDQC · Traditional Intl. Acoustics, Inc.12/07/1987SE
K864429DSP100 Carotid Phonoangiography ModuleDQC · Traditional Intl. Acoustics, Inc.05/12/1987SE
K860814DSP100 AmplifierDQC · Traditional Intl. Acoustics, Inc.12/05/1986SE

Questions and answers

When was Andries Physical Assessment Computer cleared by the FDA?

Andries Physical Assessment Computer (K870545) received a 510(k) decision of Substantially Equivalent on August 14, 1987, 185 days after the submission was received.

What is the product code of K870545?

The FDA product code is DQC – Phonocardiograph, a Class I (low risk) device regulated under 21 CFR 870.2390.