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

VDR SINUSOIDAL PERCUSIONATOR FAMILY/RELATE ACCESS

K Number: K905235 · Decision May 3, 1991
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
498
Applicant Total
11
Review Days
177

Basic Information

Device Name
VDR SINUSOIDAL PERCUSIONATOR FAMILY/RELATE ACCESS
K Number
K905235
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5895
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
PERCUSSIONAIRE CORP.
Date Received
November 7, 1990
Decision Date
May 3, 1991
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.

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Other Clearances by PERCUSSIONAIRE CORP.

K Number Device Name
K905234 TXP TRANSPORTER FAMILY AND RELATED ACCESSORIES
K905236 IPV PERCUSSIONATOR FAMILY & RELATED ACCESSORIES
K900315 PERCUSSIONAIRE TXP TRANSPORTER/RESPIRATORS 750 MIN
K900314 PERCUSSIONAIRE(R) OSCILLATRON-1 PERCUSS 1300 MIN
K900313 PERCUSSIONAIRE(R) VDR-3 IMV PERCUS/RESPIR 1250 MIN
K896586 RATE INCREASE FOR IPPB/IPV
K895485 BIRD (IPV) NONCONTINUOUS VENTILATORS
K892886 PERCUSSIONAIRE OSCILLATRON-1 MEDICAL RESPIRATOR
K895486 BIRD (VDR) SINUSOIDAL PERCUSSIONATORS
K884832 PERCUSSIONAIRE RESPIRATORS (MULTIPLE)
Search all 11 clearances from PERCUSSIONAIRE CORP. →