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

MODEL LP6 VENTILATOR, MODIFICATION

K Number: K905244 · Decision Nov 30, 1990
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
504
Applicant Total
24
Review Days
10

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
MODEL LP6 VENTILATOR, MODIFICATION
K Number
K905244
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5895
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Aequitron Medical, Inc.
Date Received
November 20, 1990
Decision Date
November 30, 1990
Product Code
CBK
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
CBK Ventilator, Continuous, Facility Use

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CBK), ordered by most recent decision date.

View all

Other Clearances by Aequitron Medical, Inc.

K Number Device Name
K961972 MODEL AMI INFANT CENTRAL APHEA/HEART RATE MONITOR
K952880 MODEL LP-1000 VOLUME VENTILATOR
K944654 OXYGEN CONCENTRATION INDICATOR
K914424 MODEL 6213 REMOTE ALARM
K915381 PORTABLE OXYGEN GENERATOR
K911399 NASAL CPAP (CONTINUOUS POSITIVE AIR PRESSURE SYST)
K903020 RESPIRATION/HEART RATE MONITOR MODEL 9500/9550
K903010 CONTINUOUS VOLUME VENTILATOR MODEL LP10
K902785 MODIFIED MODELS 9500,9550,9200,8200,HEART RATE MON
K901656 MODEL 9200 RESPIRATION/HEART RATE MONITOR
Search all 24 clearances from Aequitron Medical, Inc. →