FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

PORTABLE AIR PLETHYSMOGRAPH

K Number: K895588 · Decision Mar 27, 1990
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
113
Applicant Total
12
Review Days
193

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Basic Information

Device Name
PORTABLE AIR PLETHYSMOGRAPH
K Number
K895588
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2770
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Life Sciences Manufacturing, Inc.
Date Received
September 15, 1989
Decision Date
March 27, 1990
Product Code
DSB
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DSB Plethysmograph, Impedance

Similar 510(k) Clearances

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Other Clearances by Life Sciences Manufacturing, Inc.

K Number Device Name
K910905 SFA-II MICROPROCESSOR-CONTROLLED MODULE
K903700 IPG-II MODULE
K900365 PAG MICROPROCESSOR-CONTROLLED MODULE
K896500 CWD/PPG MODULE
K896528 SFA MODULE
K884624 MVL/MODULAB WITH PVR MODULE
K873041 A-V RECORDER
K832679 NON-INVASIVE CLINICAL VASCULAR LAB
K822522 CUTANEOUS PRESSURE PLETHYSMOGRAPH
K811560 AUTOMATED PHYSIOLOGIC PROFILE MONITOR
Search all 12 clearances from Life Sciences Manufacturing, Inc. →