Atlas FDA

PAG MICROPROCESSOR-CONTROLLED MODULE

FDA 510(k) clearance K900365 · decided 1990-07-18

Clearance details

K-number
K900365
Device name
PAG MICROPROCESSOR-CONTROLLED MODULE
Applicant
Life Sciences Manufacturing, Inc.
Decision
Substantially Equivalent
Date received
1990-01-25
Decision date
1990-07-18
Days to decision
174 days
Clearance type
Traditional
Product code
DQC
Device class
1
Regulation number
870.2390
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
West Lebanon, NH, US
Third-party review
No
Expedited review
No

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RecordFirmDate
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PHONOCARDIOGRAPH (K924054)Echo Ultrasound1993-01-22
DYNAMIC SPECTRAL PHONOCARDIOGRAPH (K902185)Reeves Scientific, Inc.1991-03-25
ACUSON HEARTSOUND/PULSE/RESPIRATION MODULE (K900560)Acuson Corp.1990-12-03
MODIFIED DSP100 AMPLIFIER (K873640)Intl. Acoustics, Inc.1987-12-07
ANDRIES PHYSICAL ASSESSMENT COMPUTER (K870545)Andries Tek, Inc.1987-08-14
DSP100 CAROTID PHONOANGIOGRAPHY MODULE (K864429)Intl. Acoustics, Inc.1987-05-12
DSP100 AMPLIFIER (K860814)Intl. Acoustics, Inc.1986-12-05
NON-INVASIVE CLINICAL VASCULAR LAB (K832679)Life Sciences Manufacturing, Inc.1984-01-03
MEDDARS/ULTRA IMAGER PULSE/PHON MODULE (K811626)Honeywell, Inc.1981-07-01

Recalls involving this device

No recalls on record reference this clearance.